Losartan Potassium
- Product NDC
- 70934-660
- 11-digit product format
- 709340660
- Labeler code
- 70934
- Product ID
- 70934-660_aca09f70-1524-14e6-e053-2a95a90ad273
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2020-04-02
- 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
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 |
|---|
| 70934-660-30 | 70934066030 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-660-30) | 2020-04-02 | 0000-00-00 | No | No | Current |