Losartan Potassium
- Product NDC
- 63629-8085
- 11-digit product format
- 636298085
- Labeler code
- 63629
- Product ID
- 63629-8085_20c244e1-fce0-41bc-aa77-a1aa35011a47
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 100 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8085-1 | 63629808501 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8085-1) | 2019-07-15 | 0000-00-00 | No | No | Current |
| 63629-8085-2 | 63629808502 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8085-2) | 2022-04-29 | 0000-00-00 | No | No | Current |