Losartan Potassium
- Product NDC
- 13668-409
- 11-digit product format
- 136680409
- Labeler code
- 13668
- Product ID
- 13668-409_dbd98acc-26f0-906a-e053-2995a90a0bc2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA090467
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13668-409-10 | 13668040910 | 1000 TABLET in 1 BOTTLE (13668-409-10) | 1000 tablet | 2010-10-06 | 0000-00-00 | No | No | Current |
| 13668-409-30 | 13668040930 | 30 TABLET in 1 BOTTLE (13668-409-30) | 30 tablet | 2010-10-06 | 0000-00-00 | No | No | Current |
| 13668-409-74 | 13668040974 | 100 TABLET in 1 CARTON (13668-409-74) | 100 tablet | 2010-10-06 | 0000-00-00 | No | No | Current |
| 13668-409-90 | 13668040990 | 90 TABLET in 1 BOTTLE (13668-409-90) | 90 tablet | 2010-10-06 | 0000-00-00 | No | No | Current |