Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 52343-116
- 11-digit product format
- 523430116
- Labeler code
- 52343
- Product ID
- 52343-116_8429d375-9e85-4dc4-870a-fc609e212a96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ACETRIS HEALTH, LLC
- Application
- ANDA091629
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
- Active strength
- 50 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
- 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 |
|---|
| 52343-116-30 | 52343011630 | 30 TABLET, FILM COATED in 1 BOTTLE (52343-116-30) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 52343-116-90 | 52343011690 | 90 TABLET, FILM COATED in 1 BOTTLE (52343-116-90) | 2010-10-06 | 0000-00-00 | No | No | Current |
| 52343-116-99 | 52343011699 | 1000 TABLET, FILM COATED in 1 BOTTLE (52343-116-99) | 2010-10-06 | 0000-00-00 | No | No | Current |