Losartan Potassium
- Product NDC
- 60760-129
- 11-digit product format
- 607600129
- Labeler code
- 60760
- Product ID
- 60760-129_7abba973-92ff-45cb-e053-2991aa0a762f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St Marys Medical Park Pharmacy
- Application
- ANDA090467
- Marketing category
- ANDA
- Marketing start
- 2013-07-11
- 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
- 2020-12-31
- 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 |
|---|
| 60760-129-90 | 60760012990 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-129-90) | 90 tablet | 2013-07-11 | 0000-00-00 | No | No | Current |