Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 57237-209
- 11-digit product format
- 572370209
- Labeler code
- 57237
- Product ID
- 57237-209_0abad334-ce8b-4f69-96d1-835a29518078
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rising Health, LLC
- Application
- ANDA091629
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- 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 |
|---|
| 57237-209-30 | 57237020930 | 30 TABLET, FILM COATED in 1 BOTTLE (57237-209-30) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 57237-209-90 | 57237020990 | 90 TABLET, FILM COATED in 1 BOTTLE (57237-209-90) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 57237-209-99 | 57237020999 | 1000 TABLET, FILM COATED in 1 BOTTLE (57237-209-99) | 2010-10-06 | 0000-00-00 | No | No | Current |