Losartan Potassium
- Product NDC
- 72603-341
- 11-digit product format
- 726030341
- Labeler code
- 72603
- Product ID
- 72603-341_40ccc1d7-14c6-e682-e063-6394a90a1d37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA203835
- Marketing category
- ANDA
- Marketing start
- 2015-08-19
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 50 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Losartan Potassium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LOSARTAN POTASSIUM | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3ST302B24A |
| Rxcui | 979480, 979485, 979492 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72603-341-01 | Losartan Potassium | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 2 |
| 72603-341-02 | Losartan Potassium | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72603-341-01 | 72603034101 | 90 TABLET, FILM COATED in 1 BOTTLE (72603-341-01) | 2015-08-19 | No | No | Current |
| 72603-341-02 | 72603034102 | 1000 TABLET, FILM COATED in 1 BOTTLE (72603-341-02) | 2015-08-19 | No | No | Current |