Hydrochlorothiazide
- Product NDC
- 71205-751
- 11-digit product format
- 712050751
- Labeler code
- 71205
- Product ID
- 71205-751_c4fe84e3-c291-4220-95c1-a2bd02b1e134
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA083177
- Marketing category
- ANDA
- Marketing start
- 1980-01-07
- 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 |
|---|
| 71205-751-30 | 71205075130 | 30 TABLET in 1 BOTTLE (71205-751-30) | 30 tablet | 2023-02-02 | No | No | Historical |
| 71205-751-60 | 71205075160 | 60 TABLET in 1 BOTTLE (71205-751-60) | 60 tablet | 2023-02-02 | No | No | Historical |
| 71205-751-90 | 71205075190 | 90 TABLET in 1 BOTTLE (71205-751-90) | 90 tablet | 2023-02-02 | No | No | Historical |