Hydrochlorothiazide
- Product NDC
- 82804-031
- 11-digit product format
- 828040031
- Labeler code
- 82804
- Product ID
- 82804-031_9dd2f58b-d143-4d0c-a298-6d9390e6187a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA040907
- Marketing category
- ANDA
- Marketing start
- 2008-08-15
- 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 |
|---|
| 82804-031-30 | 82804003130 | 30 TABLET in 1 BOTTLE (82804-031-30) | 30 tablet | 2023-10-24 | No | No | Historical |
| 82804-031-60 | 82804003160 | 60 TABLET in 1 BOTTLE (82804-031-60) | 60 tablet | 2023-10-24 | No | No | Historical |
| 82804-031-90 | 82804003190 | 90 TABLET in 1 BOTTLE (82804-031-90) | 90 tablet | 2023-10-24 | No | No | Historical |