Losartan Potassium
- Product NDC
- 70518-2786
- 11-digit product format
- 705182786
- Labeler code
- 70518
- Product ID
- 70518-2786_dc7448ab-2374-1e98-e053-2995a90aaeed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203835
- Marketing category
- ANDA
- Marketing start
- 2020-06-14
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2786-0 | 70518278600 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2786-0) | 2020-06-14 | 0000-00-00 | No | No | Current |
| 70518-2786-1 | 70518278601 | 60 TABLET, FILM COATED in 1 BLISTER PACK (70518-2786-1) | 2021-12-03 | 0000-00-00 | No | No | Current |
| 70518-2786-2 | 70518278602 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2786-2) | 2022-04-11 | 0000-00-00 | No | No | Current |