HYDROCHLOROTHIAZIDE
- Product NDC
- 71205-793
- 11-digit product format
- 712050793
- Labeler code
- 71205
- Product ID
- 71205-793_3464be28-5bab-4642-9d9b-8b425822dd07
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA085182
- Marketing category
- ANDA
- Marketing start
- 2015-01-15
- 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 |
|---|
| 71205-793-30 | 71205079330 | 30 TABLET in 1 BOTTLE (71205-793-30) | 30 tablet | 2023-04-19 | No | No | Historical |
| 71205-793-60 | 71205079360 | 60 TABLET in 1 BOTTLE (71205-793-60) | 60 tablet | 2023-04-19 | No | No | Historical |
| 71205-793-90 | 71205079390 | 90 TABLET in 1 BOTTLE (71205-793-90) | 90 tablet | 2023-04-19 | No | No | Historical |