Losartan Potassium
- Product NDC
- 70518-2132
- 11-digit product format
- 705182132
- Labeler code
- 70518
- Product ID
- 70518-2132_49d94f9d-4d6a-325c-e063-6294a90a1a8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2019-06-05
- 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
- Losartan Potassium
- 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 | 979485 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2132-0 | Losartan Potassium | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 20 |
| 70518-2132-1 | Losartan Potassium | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 20 |
| 70518-2132-2 | Losartan Potassium | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 20 |
| 70518-2132-3 | Losartan Potassium | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 20 |
| 70518-2132-4 | Losartan Potassium | 6 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 6 | | 20 |
| 70518-2132-5 | Losartan Potassium | 6 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 6 | | 20 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2132 | LOSARTAN POTASSIUM TABLET, FILM COATED [REMEDYREPACK INC.] | 16 | Current NDC, Legacy NDC, 6 package rows | 20250309_f7cf8a7d-90f1-46a3-abff-1eb316aa7d72.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 |
|---|
| 70518-2132-0 | 70518213200 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2132-0) | 2019-06-05 | 0000-00-00 | No | No | Current |
| 70518-2132-1 | 70518213201 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2132-1) | 2019-06-19 | 0000-00-00 | No | No | Current |
| 70518-2132-2 | 70518213202 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2132-2) | 2020-12-08 | 0000-00-00 | No | No | Current |
| 70518-2132-3 | 70518213203 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2132-3) | 2021-12-02 | 0000-00-00 | No | No | Current |
| 70518-2132-4 | 70518213204 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2132-4) | 2022-07-13 | 0000-00-00 | No | No | Current |
| 70518-2132-5 | 70518213205 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2132-5) | 2022-07-19 | 0000-00-00 | No | No | Current |