Losartan Potassium
- Product NDC
- 60760-125
- 11-digit product format
- 607600125
- Labeler code
- 60760
- Product ID
- 60760-125_889091bd-1aec-f5bf-e053-2a95a90a999c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2019-02-27
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-125-30 | 60760012530 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-125-30) | 2019-02-27 | 0000-00-00 | No | No | Current |
| 60760-125-90 | 60760012590 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-125-90) | 2019-02-27 | 0000-00-00 | No | No | Current |