LOSARTAN POTASSIUM
- Product NDC
- 23155-645
- 11-digit product format
- 231550645
- Labeler code
- 23155
- Product ID
- 23155-645_ab9a41fe-7b40-a543-e053-2995a90acab6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POTASSIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA090382
- Marketing category
- ANDA
- Marketing start
- 2018-01-04
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23155-645-03 | 23155064503 | 30 TABLET, FILM COATED in 1 BOTTLE (23155-645-03) | 2018-01-04 | 0000-00-00 | No | No | Current |
| 23155-645-09 | 23155064509 | 90 TABLET, FILM COATED in 1 BOTTLE (23155-645-09) | 2018-01-04 | 0000-00-00 | No | No | Current |
| 23155-645-10 | 23155064510 | 1000 TABLET, FILM COATED in 1 BOTTLE (23155-645-10) | 2018-01-04 | 0000-00-00 | No | No | Current |