Losartan potassium
- Product NDC
- 0781-5701
- 11-digit product format
- 007815701
- Labeler code
- 0781
- Product ID
- 0781-5701_e0b9eaef-95a8-42d5-8970-471d7f52e11f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA077424
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- 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
- 2020-12-31
- 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 |
|---|
| 0781-5701-01 | 00781570101 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5701-01) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 0781-5701-10 | 00781570110 | 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5701-10) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 0781-5701-31 | 00781570131 | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5701-31) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 0781-5701-74 | 00781570174 | 4000 TABLET, FILM COATED in 1 BOTTLE (0781-5701-74) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 0781-5701-92 | 00781570192 | 90 TABLET, FILM COATED in 1 BOTTLE (0781-5701-92) | 2010-10-06 | 0000-00-00 | No | No | Current |