Losartan potassium
- Product NDC
- 0781-5702
- 11-digit product format
- 007815702
- Labeler code
- 0781
- Product ID
- 0781-5702_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
- 100 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 |
|---|
| 0781-5702-01 | 00781570201 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5702-01) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 0781-5702-10 | 00781570210 | 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5702-10) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 0781-5702-31 | 00781570231 | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5702-31) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 0781-5702-92 | 00781570292 | 90 TABLET, FILM COATED in 1 BOTTLE (0781-5702-92) | 2010-10-06 | 0000-00-00 | No | No | Current |