HYDROCHLOROTHIAZIDE
- Product NDC
- 71610-471
- 11-digit product format
- 716100471
- Labeler code
- 71610
- Product ID
- 71610-471_b9ef366b-1b6f-4060-a3f0-6c6f5399144e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA040702
- Marketing category
- ANDA
- Marketing start
- 2007-03-16
- 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 |
|---|
| 71610-471-45 | 71610047145 | 45 TABLET in 1 BOTTLE, PLASTIC (71610-471-45) | 45 tablet | 2020-10-09 | No | No | Historical |
| 71610-471-60 | 71610047160 | 90 TABLET in 1 BOTTLE, PLASTIC (71610-471-60) | 90 tablet | 2020-10-09 | No | No | Historical |