NDC 63629-2912
COZAAR
Losartan Potassium
COZAAR is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Losartan Potassium.
| Product ID | 63629-2912_b3441dee-4369-461d-9868-798de86960fa |
| NDC | 63629-2912 |
| Product Type | Human Prescription Drug |
| Proprietary Name | COZAAR |
| Generic Name | Losartan Potassium |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1995-04-14 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020386 |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | LOSARTAN POTASSIUM |
| Active Ingredient Strength | 100 mg/1 |
| Pharm Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 63629-2912-4
100 TABLET, FILM COATED in 1 BOTTLE (63629-2912-4)
| Marketing Start Date | 1995-04-14 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 63629-2912-4 [63629291204]
COZAAR TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020386 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-23 |
| Marketing End Date | 2009-10-01 |
NDC 63629-2912-3 [63629291203]
COZAAR TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020386 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-23 |
| Marketing End Date | 2009-10-01 |
NDC 63629-2912-2 [63629291202]
COZAAR TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020386 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-23 |
| Marketing End Date | 2009-10-01 |
NDC 63629-2912-1 [63629291201]
COZAAR TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA020386 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-02-23 |
| Marketing End Date | 2009-10-01 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| LOSARTAN POTASSIUM | 100 mg/1 |
OpenFDA Data
| SPL SET ID: | 3f60ac2e-031a-48fa-ab47-4e3aec49cb83 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
Pharmacological Class
- Angiotensin 2 Receptor Antagonists [MoA]
- Angiotensin 2 Receptor Blocker [EPC]
NDC Crossover Matching brand name "COZAAR" or generic name "Losartan Potassium"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0006-0951 | COZAAR | losartan potassium |
| 0006-0952 | COZAAR | losartan potassium |
| 0006-0960 | COZAAR | losartan potassium |
| 55289-238 | COZAAR | COZAAR |
| 63629-2912 | COZAAR | COZAAR |
| 0054-0123 | Losartan Potassium | Losartan Potassium |
| 0054-0124 | Losartan Potassium | Losartan Potassium |
| 0054-0125 | Losartan Potassium | Losartan Potassium |
| 0093-7364 | Losartan Potassium | Losartan Potassium |
| 0093-7365 | Losartan Potassium | Losartan Potassium |
| 0093-7366 | Losartan Potassium | Losartan Potassium |
| 0179-0200 | Losartan Potassium | Losartan Potassium |
| 0179-0202 | Losartan Potassium | Losartan Potassium |
| 0179-0203 | Losartan Potassium | Losartan Potassium |
| 0615-7604 | Losartan Potassium | Losartan Potassium |
| 0615-7605 | Losartan Potassium | Losartan Potassium |
| 0615-7606 | Losartan Potassium | Losartan Potassium |
| 0615-7958 | Losartan Potassium | Losartan Potassium |
| 0615-7959 | Losartan Potassium | Losartan Potassium |
| 0615-7960 | Losartan Potassium | Losartan Potassium |
| 0615-8207 | Losartan Potassium | Losartan Potassium |
| 0615-8208 | Losartan Potassium | Losartan Potassium |
| 0615-8209 | Losartan Potassium | Losartan Potassium |
| 0781-5700 | Losartan potassium | losartan potassium |
| 0781-5701 | Losartan potassium | losartan potassium |
| 0781-5702 | Losartan potassium | losartan potassium |
Trademark Results [COZAAR]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 COZAAR 74193404 1805072 Live/Registered |
MERCK SHARP & DOHME CORP. 1991-08-12 |
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