Hydrochlorothiazide
- Product NDC
- 63629-1220
- 11-digit product format
- 636291220
- Labeler code
- 63629
- Product ID
- 63629-1220_0803d298-8a74-ebee-e063-6394a90aecc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2002-03-29
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 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 |
|---|
| 63629-1220-1 | 63629122001 | 100 TABLET in 1 BOTTLE (63629-1220-1) | 100 tablet | 2021-01-14 | No | No | Historical |