Hydrochlorothiazide
- Product NDC
- 60429-889
- 11-digit product format
- 604290889
- Labeler code
- 60429
- Product ID
- 60429-889_e2707001-f962-ebd5-e053-2995a90a2de1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA083177
- Marketing category
- ANDA
- Marketing start
- 1973-01-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-889-01 | 60429088901 | 100 TABLET in 1 BOTTLE (60429-889-01) | 100 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |
| 60429-889-10 | 60429088910 | 1000 TABLET in 1 BOTTLE (60429-889-10) | 1000 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |
| 60429-889-90 | 60429088990 | 90 TABLET in 1 BOTTLE (60429-889-90) | 90 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |