Losartan Potassium
- Product NDC
- 68788-7914
- 11-digit product format
- 687887914
- Labeler code
- 68788
- Product ID
- 68788-7914_21abee77-536d-4750-9916-03daf33af1fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078232
- Marketing category
- ANDA
- Marketing start
- 2021-05-19
- 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
- 2023-12-31
- 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 |
|---|
| 68788-7914-1 | 68788791401 | 100 TABLET in 1 BOTTLE (68788-7914-1) | 100 tablet | 2021-05-19 | 0000-00-00 | No | No | Current |
| 68788-7914-3 | 68788791403 | 30 TABLET in 1 BOTTLE (68788-7914-3) | 30 tablet | 2021-05-19 | 0000-00-00 | No | No | Current |
| 68788-7914-6 | 68788791406 | 60 TABLET in 1 BOTTLE (68788-7914-6) | 60 tablet | 2021-05-19 | 0000-00-00 | No | No | Current |
| 68788-7914-9 | 68788791409 | 90 TABLET in 1 BOTTLE (68788-7914-9) | 90 tablet | 2021-05-19 | 0000-00-00 | No | No | Current |