Losartan Potassium
- Product NDC
- 70518-1795
- 11-digit product format
- 705181795
- Labeler code
- 70518
- Product ID
- 70518-1795_ea4d457f-8ea6-a243-e053-2a95a90a6584
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2019-01-11
- 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 |
|---|
| 70518-1795-0 | 70518179500 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1795-0) | 2019-01-11 | 0000-00-00 | No | No | Current |
| 70518-1795-1 | 70518179501 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1795-1) | 2022-10-05 | 0000-00-00 | No | No | Current |