Losartan Potassium
- Product NDC
- 55154-7631
- 11-digit product format
- 551547631
- Labeler code
- 55154
- Product ID
- 55154-7631_fc7c3523-a0f4-43c3-9789-1710efb9f91c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA090467
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- 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
- 2021-12-31
- 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 |
|---|
| 55154-7631-0 | 55154763100 | 10 BLISTER PACK in 1 BAG (55154-7631-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2010-10-06 | 0000-00-00 | No | No | Current |