Losortan Potassium
- Product NDC
- 63629-4238
- 11-digit product format
- 636294238
- Labeler code
- 63629
- Product ID
- 63629-4238_a4644f7f-ccb3-5ef5-1a08-f6daa6e77f6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078243
- Marketing category
- ANDA
- Marketing start
- 2010-10-04
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-4238-1 | 63629423801 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4238-1) | 2011-01-25 | 0000-00-00 | No | No | Current |
| 63629-4238-2 | 63629423802 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-4238-2) | 2011-01-25 | 0000-00-00 | No | No | Current |
| 63629-4238-3 | 63629423803 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-4238-3) | 2012-10-17 | 0000-00-00 | No | No | Current |
| 63629-4238-4 | 63629423804 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-4238-4) | 2011-01-04 | 0000-00-00 | No | No | Current |
| 63629-4238-5 | 63629423805 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-4238-5) | 2014-10-06 | 0000-00-00 | No | No | Current |
| 63629-4238-6 | 63629423806 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-4238-6) | 2022-02-08 | 0000-00-00 | No | No | Current |
| 63629-4238-7 | 63629423807 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-4238-7) | 2022-02-08 | 0000-00-00 | No | No | Current |