LOSARTAN POTASSIUM
- Product NDC
- 70518-2530
- 11-digit product format
- 705182530
- Labeler code
- 70518
- Product ID
- 70518-2530_dc1635c0-ffdd-e1c9-e053-2a95a90a4b86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POTASSIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090382
- Marketing category
- ANDA
- Marketing start
- 2020-01-07
- 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 |
|---|
| 70518-2530-0 | 70518253000 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2530-0) | 2020-01-07 | 0000-00-00 | No | No | Current |