Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 50090-5295
- 11-digit product format
- 500905295
- Labeler code
- 50090
- Product ID
- 50090-5295_f4ce2db1-0c81-486d-918a-5a3d27adba8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077157
- Marketing category
- ANDA
- Marketing start
- 2010-04-06
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
- Active strength
- 100 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5295-0 | 50090529500 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-5295-0) | 2020-10-26 | 0000-00-00 | No | No | Current |
| 50090-5295-1 | 50090529501 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5295-1) | 2020-10-26 | 0000-00-00 | No | No | Current |