Hydrochlorothiazide
- Product NDC
- 68788-8126
- 11-digit product format
- 687888126
- Labeler code
- 68788
- Product ID
- 68788-8126_62bdfe20-2cf5-434e-aa56-98729bba03ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA087059
- Marketing category
- ANDA
- Marketing start
- 2022-01-17
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8126-0 | 68788812600 | 100 TABLET in 1 BOTTLE (68788-8126-0) | 100 tablet | 2022-01-17 | 0000-00-00 | No | No | Current |
| 68788-8126-1 | 68788812601 | 15 TABLET in 1 BOTTLE (68788-8126-1) | 15 tablet | 2022-01-17 | 0000-00-00 | No | No | Current |
| 68788-8126-3 | 68788812603 | 30 TABLET in 1 BOTTLE (68788-8126-3) | 30 tablet | 2022-01-17 | 0000-00-00 | No | No | Current |
| 68788-8126-6 | 68788812606 | 60 TABLET in 1 BOTTLE (68788-8126-6) | 60 tablet | 2022-01-17 | 0000-00-00 | No | No | Current |
| 68788-8126-9 | 68788812609 | 90 TABLET in 1 BOTTLE (68788-8126-9) | 90 tablet | 2022-01-17 | 0000-00-00 | No | No | Current |