HYDROCHLOROTHIAZIDE
- Product NDC
- 60760-430
- 11-digit product format
- 607600430
- Labeler code
- 60760
- Product ID
- 60760-430_affe4a45-9d75-8904-e053-2995a90a6a57
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA085182
- Marketing category
- ANDA
- Marketing start
- 2015-01-15
- 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
- 2021-12-31
- 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 |
|---|
| 60760-430-30 | 60760043030 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-430-30) | 30 tablet | 2020-08-05 | 0000-00-00 | No | No | Current |
| 60760-430-90 | 60760043090 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-430-90) | 90 tablet | 2020-05-27 | 0000-00-00 | No | No | Current |