Losartan Potassium
- Product NDC
- 68788-7470
- 11-digit product format
- 687887470
- Labeler code
- 68788
- Product ID
- 68788-7470_6e7b77b5-e93e-4c6e-9fbd-0a7a57d75291
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2020-02-28
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 68788-7470-1 | 68788747001 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7470-1) | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7470-3 | 68788747003 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7470-3) | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7470-5 | 68788747005 | 50 TABLET, FILM COATED in 1 BOTTLE (68788-7470-5) | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7470-6 | 68788747006 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7470-6) | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7470-9 | 68788747009 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7470-9) | 2020-02-28 | 0000-00-00 | No | No | Current |