Hydrochlorothiazide
- Product NDC
- 63629-1121
- 11-digit product format
- 636291121
- Labeler code
- 63629
- Product ID
- 63629-1121_347d6500-0340-4c07-bb2e-6d513b0abdd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2002-03-29
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 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 |
|---|
| 63629-1121-1 | 63629112101 | 1000 TABLET in 1 BOTTLE, PLASTIC (63629-1121-1) | 1000 tablet | 2002-03-29 | 0000-00-00 | No | No | Current |