Hydrochlorothiazide
- Product NDC
- 70518-4113
- 11-digit product format
- 705184113
- Labeler code
- 70518
- Product ID
- 70518-4113_3c554e53-4fe4-5d93-e063-6394a90a1901
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA087059
- Marketing category
- ANDA
- Marketing start
- 2024-06-26
- 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 |
|---|
| 70518-4113-0 | 70518411300 | 30 TABLET in 1 BLISTER PACK (70518-4113-0) | 30 tablet | 2024-06-26 | No | No | Historical |