Hydrochlorothiazide
- Product NDC
- 68071-2405
- 11-digit product format
- 680712405
- Labeler code
- 68071
- Product ID
- 68071-2405_4ddbc48d-4b16-547e-e063-6294a90a0d34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2013-04-10
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 68071-2405-1 | 68071240501 | 100 TABLET in 1 BOTTLE (68071-2405-1) | 100 tablet | 2021-05-21 | No | No | Historical |