Losartan Potassium
- Product NDC
- 0054-0124
- 11-digit product format
- 000540124
- Labeler code
- 0054
- Product ID
- 0054-0124_856bc6e8-6f23-48cd-a2b7-d222c3f99913
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA077459
- Marketing category
- ANDA
- Marketing start
- 2020-07-13
- 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 |
|---|
| 0054-0124-22 | 00054012422 | 90 TABLET in 1 BOTTLE (0054-0124-22) | 90 tablet | 2010-10-06 | 0000-00-00 | No | No | Current |