Losartan potassium Tablets, 50 mg
- Product NDC
- 63629-2427
- 11-digit product format
- 636292427
- Labeler code
- 63629
- Product ID
- 63629-2427_26db1376-0bdd-42b4-81c1-b5b0f83b03dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201170
- Marketing category
- ANDA
- Marketing start
- 2012-09-18
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2427-1 | 63629242701 | 1000 TABLET in 1 BOTTLE (63629-2427-1) | 1000 tablet | 2021-02-25 | 0000-00-00 | No | No | Current |