Losartan Potassium
- Product NDC
- 0904-6391
- 11-digit product format
- 009046391
- Labeler code
- 0904
- Product ID
- 0904-6391_77df2a91-b42d-42e6-a9cf-202e12a4482d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA090467
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 2021-08-31
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 25 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0904-6391-61 | 00904639161 | 100 BLISTER PACK in 1 CARTON (0904-6391-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2010-10-06 | 2021-08-31 | No | No | Current |