Hydrochlorothiazide
- Product NDC
- 50090-5333
- 11-digit product format
- 500905333
- Labeler code
- 50090
- Product ID
- 50090-5333_21d6b8fe-8c6e-4584-a091-d5ccd1984865
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2013-04-10
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0J48LPH2TH | HYDROCHLOROTHIAZIDE | 58-93-5 | HYDROCHLOROTHIAZIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-5333-0 | 50090533300 | 90 TABLET in 1 BOTTLE (50090-5333-0) | 90 tablet | 2020-11-03 | No | No | Historical |