HYDROCHLOROTHIAZIDE
- Product NDC
- 70518-3780
- 11-digit product format
- 705183780
- Labeler code
- 70518
- Product ID
- 70518-3780_348bc808-7a18-4706-e063-6294a90ab7b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA085182
- Marketing category
- ANDA
- Marketing start
- 2023-07-09
- 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 |
|---|
| 70518-3780-0 | 70518378000 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3780-0) | 90 tablet | 2023-07-09 | No | No | Historical |
| 70518-3780-1 | 70518378001 | 30 TABLET in 1 BLISTER PACK (70518-3780-1) | 30 tablet | 2023-12-08 | No | No | Historical |