Hydrochlorothiazide
- Product NDC
- 60429-888
- 11-digit product format
- 604290888
- Labeler code
- 60429
- Product ID
- 60429-888_ebcd382d-5637-585c-e053-2995a90aa86c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA040707
- Marketing category
- ANDA
- Marketing start
- 2007-02-27
- Marketing end
- 2023-03-31
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 60429-888-01 | 60429088801 | 100 TABLET in 1 BOTTLE (60429-888-01) | 100 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |