COZAAR
- Product NDC
- 78206-121
- 11-digit product format
- 782060121
- Labeler code
- 78206
- Product ID
- 78206-121_998b309b-7dde-4d62-b902-010dd83108fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Organon LLC
- Application
- NDA020386
- Marketing category
- NDA
- Marketing start
- 2021-06-01
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 25 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- COZAAR
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LOSARTAN POTASSIUM | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3ST302B24A |
| Rxcui | 979480, 979482, 979485, 979487, 979492, 979494 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 78206-121-01 | COZAAR | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 78206-121 | COZAAR (LOSARTAN POTASSIUM) TABLET, FILM COATED [ORGANON LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241123_9949448f-c3b9-44ee-94ed-c1aca8c90f39.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 78206-121-01 | 78206012101 | 90 TABLET, FILM COATED in 1 BOTTLE (78206-121-01) | 2021-06-01 | 0000-00-00 | No | No | Current |