Losartan Potassium
- Product NDC
- 63187-935
- 11-digit product format
- 631870935
- Labeler code
- 63187
- Product ID
- 63187-935_90f98130-7530-4edd-b293-9a96f179eb67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076958
- Marketing category
- ANDA
- Marketing start
- 2010-04-06
- 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 |
|---|
| 63187-935-30 | 63187093530 | 30 TABLET, FILM COATED in 1 BOTTLE (63187-935-30) | 2017-12-01 | 0000-00-00 | No | No | Current |
| 63187-935-60 | 63187093560 | 60 TABLET, FILM COATED in 1 BOTTLE (63187-935-60) | 2017-12-01 | 0000-00-00 | No | No | Current |
| 63187-935-90 | 63187093590 | 90 TABLET, FILM COATED in 1 BOTTLE (63187-935-90) | 2017-12-01 | 0000-00-00 | No | No | Current |