Hydrochlorothiazide
- Product NDC
- 50090-6988
- 11-digit product format
- 500906988
- Labeler code
- 50090
- Product ID
- 50090-6988_46f6397e-cc46-44f8-88d1-0004e657304d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203561
- Marketing category
- ANDA
- Marketing start
- 2019-01-14
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 12.5 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 |
|---|
| 50090-6988-0 | 50090698800 | 90 CAPSULE in 1 BOTTLE (50090-6988-0) | 90 capsule | 2023-12-27 | No | No | Historical |