100 results for pfizer
| ApplNo | Type | Drug Name | Active Ingredient | Form / Strength | Marketing Status | TE | Sponsor |
|---|---|---|---|---|---|---|---|
| 761118 | BLA | ABRILADA | ADALIMUMAB-AFZB | INJECTABLE;INJECTION — 40MG/0.8ML | Prescription | PFIZER INC | |
| 761118 | BLA | ABRILADA | ADALIMUMAB-AFZB | INJECTABLE;INJECTION — 20MG/0.4ML | Prescription | PFIZER INC | |
| 761118 | BLA | ABRILADA | ADALIMUMAB-AFZB | INJECTABLE;INJECTION — 10MG/0.2ML | Prescription | PFIZER INC | |
| 019885 | NDA | ACCUPRIL | QUINAPRIL HYDROCHLORIDE | TABLET;ORAL — EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | AB | PFIZER PHARMS |
| 019885 | NDA | ACCUPRIL | QUINAPRIL HYDROCHLORIDE | TABLET;ORAL — EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | AB | PFIZER PHARMS |
| 019885 | NDA | ACCUPRIL | QUINAPRIL HYDROCHLORIDE | TABLET;ORAL — EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | AB | PFIZER PHARMS |
| 019885 | NDA | ACCUPRIL | QUINAPRIL HYDROCHLORIDE | TABLET;ORAL — EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | AB | PFIZER PHARMS |
| 020125 | NDA | ACCURETIC | HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE | TABLET;ORAL — 12.5MG;EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | AB | PFIZER PHARMS |
| 020125 | NDA | ACCURETIC | HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE | TABLET;ORAL — 12.5MG;EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | AB | PFIZER PHARMS |
| 020125 | NDA | ACCURETIC | HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE | TABLET;ORAL — 25MG;EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | AB | PFIZER PHARMS |
| 063165 | ANDA | ADRIAMYCIN PFS | DOXORUBICIN HYDROCHLORIDE | INJECTABLE;INJECTION — 2MG/ML | Discontinued | PFIZER | |
| 063165 | ANDA | ADRIAMYCIN PFS | DOXORUBICIN HYDROCHLORIDE | INJECTABLE;INJECTION — 200MG/100ML | Discontinued | PFIZER | |
| 012616 | NDA | ALDACTAZIDE | HYDROCHLOROTHIAZIDE; SPIRONOLACTONE | TABLET;ORAL — 25MG;25MG | Prescription | AB | PFIZER |
| 012616 | NDA | ALDACTAZIDE | HYDROCHLOROTHIAZIDE; SPIRONOLACTONE | TABLET;ORAL — 50MG;50MG | Discontinued | PFIZER | |
| 012151 | NDA | ALDACTONE | SPIRONOLACTONE | TABLET;ORAL — 50MG | Prescription | AB | PFIZER |
| 012151 | NDA | ALDACTONE | SPIRONOLACTONE | TABLET;ORAL — 25MG | Prescription | AB | PFIZER |
| 012151 | NDA | ALDACTONE | SPIRONOLACTONE | TABLET;ORAL — 100MG | Prescription | AB | PFIZER |
| 022021 | NDA | ALTACE | RAMIPRIL | TABLET;ORAL — 1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | KING PFIZER | |
| 022021 | NDA | ALTACE | RAMIPRIL | TABLET;ORAL — 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | KING PFIZER | |
| 022021 | NDA | ALTACE | RAMIPRIL | TABLET;ORAL — 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | KING PFIZER | |
| 022021 | NDA | ALTACE | RAMIPRIL | TABLET;ORAL — 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | KING PFIZER | |
| 020753 | NDA | AROMASIN | EXEMESTANE | TABLET;ORAL — 25MG | Prescription | AB | PFIZER |
| 020607 | NDA | ARTHROTEC | DICLOFENAC SODIUM; MISOPROSTOL | TABLET, DELAYED RELEASE;ORAL — 50MG;0.2MG | Prescription | AB | PFIZER |
| 020607 | NDA | ARTHROTEC | DICLOFENAC SODIUM; MISOPROSTOL | TABLET, DELAYED RELEASE;ORAL — 75MG;0.2MG | Prescription | AB | PFIZER |
| 010392 | NDA | ATARAX | HYDROXYZINE HYDROCHLORIDE | TABLET;ORAL — 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 010392 | NDA | ATARAX | HYDROXYZINE HYDROCHLORIDE | TABLET;ORAL — 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 010392 | NDA | ATARAX | HYDROXYZINE HYDROCHLORIDE | TABLET;ORAL — 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 010392 | NDA | ATARAX | HYDROXYZINE HYDROCHLORIDE | TABLET;ORAL — 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 007073 | NDA | AZULFIDINE | SULFASALAZINE | TABLET;ORAL — 500MG | Prescription | AB | PFIZER |
| 007073 | NDA | AZULFIDINE EN-TABS | SULFASALAZINE | TABLET, DELAYED RELEASE;ORAL — 500MG | Prescription | AB | PFIZER |
| 018817 | NDA | CALAN | VERAPAMIL HYDROCHLORIDE | TABLET;ORAL — 80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 018817 | NDA | CALAN | VERAPAMIL HYDROCHLORIDE | TABLET;ORAL — 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 018817 | NDA | CALAN | VERAPAMIL HYDROCHLORIDE | TABLET;ORAL — 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 018817 | NDA | CALAN | VERAPAMIL HYDROCHLORIDE | TABLET;ORAL — 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 019152 | NDA | CALAN SR | VERAPAMIL HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL — 240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | AB | PFIZER |
| 019152 | NDA | CALAN SR | VERAPAMIL HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL — 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 019152 | NDA | CALAN SR | VERAPAMIL HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL — 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | AB | PFIZER |
| 020571 | NDA | CAMPTOSAR | IRINOTECAN HYDROCHLORIDE | INJECTABLE;INJECTION — 40MG/2ML (20MG/ML) | Prescription | AP | PFIZER INC |
| 020571 | NDA | CAMPTOSAR | IRINOTECAN HYDROCHLORIDE | INJECTABLE;INJECTION — 100MG/5ML (20MG/ML) | Prescription | AP | PFIZER INC |
| 020571 | NDA | CAMPTOSAR | IRINOTECAN HYDROCHLORIDE | INJECTABLE;INJECTION — 300MG/15ML (20MG/ML) | Prescription | AP | PFIZER INC |
| 020379 | NDA | CAVERJECT | ALPROSTADIL | INJECTABLE;INJECTION — 0.01MG/VIAL | Prescription | AP | PFIZER |
| 020379 | NDA | CAVERJECT | ALPROSTADIL | INJECTABLE;INJECTION — 0.02MG/VIAL | Prescription | AP | PFIZER |
| 020379 | NDA | CAVERJECT | ALPROSTADIL | INJECTABLE;INJECTION — 0.005MG/VIAL | Discontinued | PFIZER | |
| 020379 | NDA | CAVERJECT | ALPROSTADIL | INJECTABLE;INJECTION — 0.04MG/VIAL | Prescription | AP | PFIZER |
| 020755 | NDA | CAVERJECT | ALPROSTADIL | INJECTABLE;INJECTION — 0.005MG/ML | Discontinued | PFIZER | |
| 020755 | NDA | CAVERJECT | ALPROSTADIL | INJECTABLE;INJECTION — 0.01MG/ML | Discontinued | PFIZER | |
| 020755 | NDA | CAVERJECT | ALPROSTADIL | INJECTABLE;INJECTION — 0.02MG/ML | Discontinued | PFIZER | |
| 021212 | NDA | CAVERJECT IMPULSE | ALPROSTADIL | INJECTABLE;INJECTION — 0.01MG/VIAL | Prescription | PFIZER | |
| 021212 | NDA | CAVERJECT IMPULSE | ALPROSTADIL | INJECTABLE;INJECTION — 0.02MG/VIAL | Prescription | PFIZER | |
| 050551 | NDA | CEFOBID | CEFOPERAZONE SODIUM | INJECTABLE;INJECTION — EQ 1GM BASE/VIAL | Discontinued | PFIZER | |
| 050551 | NDA | CEFOBID | CEFOPERAZONE SODIUM | INJECTABLE;INJECTION — EQ 2GM BASE/VIAL | Discontinued | PFIZER | |
| 050551 | NDA | CEFOBID | CEFOPERAZONE SODIUM | INJECTABLE;INJECTION — EQ 10GM BASE/VIAL | Discontinued | PFIZER | |
| 063333 | ANDA | CEFOBID | CEFOPERAZONE SODIUM | INJECTABLE;INJECTION — EQ 1GM BASE/VIAL | Discontinued | PFIZER | |
| 063333 | ANDA | CEFOBID | CEFOPERAZONE SODIUM | INJECTABLE;INJECTION — EQ 2GM BASE/VIAL | Discontinued | PFIZER | |
| 050613 | NDA | CEFOBID IN PLASTIC CONTAINER | CEFOPERAZONE SODIUM | INJECTABLE;INJECTION — EQ 40MG BASE/ML | Discontinued | PFIZER | |
| 050613 | NDA | CEFOBID IN PLASTIC CONTAINER | CEFOPERAZONE SODIUM | INJECTABLE;INJECTION — EQ 20MG BASE/ML | Discontinued | PFIZER | |
| 213871 | NDA | CIBINQO | ABROCITINIB | TABLET;ORAL — 50MG | Prescription | PFIZER | |
| 213871 | NDA | CIBINQO | ABROCITINIB | TABLET;ORAL — 100MG | Prescription | PFIZER | |
| 213871 | NDA | CIBINQO | ABROCITINIB | TABLET;ORAL — 200MG | Prescription | PFIZER | |
| 050537 | NDA | CLEOCIN | CLINDAMYCIN PHOSPHATE | SWAB;TOPICAL — EQ 1% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 050680 | NDA | CLEOCIN | CLINDAMYCIN PHOSPHATE | CREAM;VAGINAL — EQ 2% BASE | Discontinued | PFIZER | |
| 050680 | NDA | CLEOCIN | CLINDAMYCIN PHOSPHATE | CREAM;VAGINAL — EQ 2% BASE | Prescription | AB | PFIZER |
| 050767 | NDA | CLEOCIN | CLINDAMYCIN PHOSPHATE | SUPPOSITORY;VAGINAL — 100MG | Prescription | PFIZER | |
| 062644 | ANDA | CLEOCIN | CLINDAMYCIN PALMITATE HYDROCHLORIDE | FOR SOLUTION;ORAL — EQ 75MG BASE/5ML | Prescription | AA | PFIZER |
| 050162 | NDA | CLEOCIN HYDROCHLORIDE | CLINDAMYCIN HYDROCHLORIDE | CAPSULE;ORAL — EQ 75MG BASE | Prescription | AB | PFIZER |
| 050162 | NDA | CLEOCIN HYDROCHLORIDE | CLINDAMYCIN HYDROCHLORIDE | CAPSULE;ORAL — EQ 150MG BASE | Prescription | AB | PFIZER |
| 050162 | NDA | CLEOCIN HYDROCHLORIDE | CLINDAMYCIN HYDROCHLORIDE | CAPSULE;ORAL — EQ 300MG BASE | Prescription | AB | PFIZER |
| 050441 | NDA | CLEOCIN PHOSPHATE | CLINDAMYCIN PHOSPHATE | INJECTABLE;INJECTION — EQ 150MG BASE/ML | Prescription | AP | PFIZER |
| 062803 | ANDA | CLEOCIN PHOSPHATE | CLINDAMYCIN PHOSPHATE | INJECTABLE;INJECTION — EQ 150MG BASE/ML | Prescription | AP | PFIZER |
| 050639 | NDA | CLEOCIN PHOSPHATE IN DEXTROSE 5% IN PLASTIC CONTAINER | CLINDAMYCIN PHOSPHATE | INJECTABLE;INJECTION — EQ 6MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 050639 | NDA | CLEOCIN PHOSPHATE IN DEXTROSE 5% IN PLASTIC CONTAINER | CLINDAMYCIN PHOSPHATE | INJECTABLE;INJECTION — EQ 12MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 050639 | NDA | CLEOCIN PHOSPHATE IN DEXTROSE 5% IN PLASTIC CONTAINER | CLINDAMYCIN PHOSPHATE | INJECTABLE;INJECTION — EQ 18MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 050537 | NDA | CLEOCIN T | CLINDAMYCIN PHOSPHATE | SOLUTION;TOPICAL — EQ 1% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | PFIZER | |
| 050600 | NDA | CLEOCIN T | CLINDAMYCIN PHOSPHATE | LOTION;TOPICAL — EQ 1% BASE | Prescription | AB | PFIZER |
| 050615 | NDA | CLEOCIN T | CLINDAMYCIN PHOSPHATE | GEL;TOPICAL — EQ 1% BASE | Prescription | AB1 | PFIZER |
| 017563 | NDA | COLESTID | COLESTIPOL HYDROCHLORIDE | GRANULE;ORAL — 5GM/SCOOPFUL | Prescription | AB | PFIZER |
| 017563 | NDA | COLESTID | COLESTIPOL HYDROCHLORIDE | GRANULE;ORAL — 5GM/PACKET | Prescription | AB | PFIZER |
| 020222 | NDA | COLESTID | COLESTIPOL HYDROCHLORIDE | TABLET;ORAL — 1GM | Prescription | AB | PFIZER |
| 009127 | NDA | CORTRIL | HYDROCORTISONE | TABLET;ORAL — 20MG | Discontinued | PFIZER | |
| 009127 | NDA | CORTRIL | HYDROCORTISONE | TABLET;ORAL — 10MG | Discontinued | PFIZER | |
| 009164 | NDA | CORTRIL | HYDROCORTISONE ACETATE | INJECTABLE;INJECTION — 25MG/ML | Discontinued | PFIZER | |
| 009176 | NDA | CORTRIL | HYDROCORTISONE | OINTMENT;TOPICAL — 1% | Discontinued | PFIZER GLOBAL | |
| 009176 | NDA | CORTRIL | HYDROCORTISONE | OINTMENT;TOPICAL — 2.5% | Discontinued | PFIZER GLOBAL | |
| 020491 | NDA | CORVERT | IBUTILIDE FUMARATE | INJECTABLE;INJECTION — 0.1MG/ML | Prescription | AP | PFIZER |
| 020552 | NDA | COVERA-HS | VERAPAMIL HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL — 180MG | Discontinued | PFIZER | |
| 020552 | NDA | COVERA-HS | VERAPAMIL HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL — 240MG | Discontinued | PFIZER | |
| 019281 | NDA | CYKLOKAPRON | TRANEXAMIC ACID | INJECTABLE;INJECTION — 100MG/ML | Prescription | AP | PFIZER |
| 019268 | NDA | CYTOTEC | MISOPROSTOL | TABLET;ORAL — 0.2MG | Prescription | AB | PFIZER |
| 019268 | NDA | CYTOTEC | MISOPROSTOL | TABLET;ORAL — 0.1MG | Prescription | AB | PFIZER |
| 011612 | NDA | DARICON | OXYPHENCYCLIMINE HYDROCHLORIDE | TABLET;ORAL — 10MG | Discontinued | PFIZER | |
| 210656 | NDA | DAURISMO | GLASDEGIB MALEATE | TABLET;ORAL — EQ 25MG BASE | Prescription | PFIZER | |
| 210656 | NDA | DAURISMO | GLASDEGIB MALEATE | TABLET;ORAL — EQ 100MG BASE | Prescription | PFIZER | |
| 018841 | NDA | DAYPRO | OXAPROZIN | TABLET;ORAL — 600MG | Discontinued | AB | PFIZER |
| 020776 | NDA | DAYPRO ALTA | OXAPROZIN POTASSIUM | TABLET;ORAL — 600MG | Discontinued | PFIZER | |
| 085470 | ANDA | DEPO-ESTRADIOL | ESTRADIOL CYPIONATE | INJECTABLE;INJECTION — 1MG/ML | Discontinued | PFIZER | |
| 085470 | ANDA | DEPO-ESTRADIOL | ESTRADIOL CYPIONATE | INJECTABLE;INJECTION — 3MG/ML | Discontinued | PFIZER | |
| 085470 | ANDA | DEPO-ESTRADIOL | ESTRADIOL CYPIONATE | INJECTABLE;INJECTION — 5MG/ML | Prescription | PFIZER | |
| 011757 | NDA | DEPO-MEDROL | METHYLPREDNISOLONE ACETATE | INJECTABLE;INJECTION — 40MG/ML | Prescription | AB | PFIZER |
| 011757 | NDA | DEPO-MEDROL | METHYLPREDNISOLONE ACETATE | INJECTABLE;INJECTION — 20MG/ML | Prescription | AB | PFIZER |
| 011757 | NDA | DEPO-MEDROL | METHYLPREDNISOLONE ACETATE | INJECTABLE;INJECTION — 80MG/ML | Prescription | AB | PFIZER |