Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 50090-1176
- 11-digit product format
- 500901176
- Labeler code
- 50090
- Product ID
- 50090-1176_c2612c58-66a4-41d7-a085-107b86d686d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090528
- 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
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50090-1176-0 | 50090117600 | 30 TABLET in 1 BOTTLE (50090-1176-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1176-1 | 50090117601 | 90 TABLET in 1 BOTTLE (50090-1176-1) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |