Losartan Potassium
- Product NDC
- 63629-8086
- 11-digit product format
- 636298086
- Labeler code
- 63629
- Product ID
- 63629-8086_478f0665-7754-421a-88dc-a38fab081a7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- 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
- 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 |
|---|
| 63629-8086-1 | 63629808601 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8086-1) | 2019-07-25 | 0000-00-00 | No | No | Current |