Losartan potassium
- Product NDC
- 70934-932
- 11-digit product format
- 709340932
- Labeler code
- 70934
- Product ID
- 70934-932_d39a14e3-a4b3-337b-e053-2995a90a35b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA202230
- Marketing category
- ANDA
- Marketing start
- 2021-12-09
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 100 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70934-932-90 | 70934093290 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-932-90) | 2021-12-09 | 0000-00-00 | No | No | Current |