LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
- Product NDC
- 72189-139
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA201845
- Marketing category
- ANDA
- Substance
- HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72189-139-30 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-139-30) | 2020-12-02 | | No | Historical |
| 72189-139-90 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-139-90) | 2020-12-02 | | No | Historical |