Hydrochlorothiazide
- Product NDC
- 63629-8233
- 11-digit product format
- 636298233
- Labeler code
- 63629
- Product ID
- 63629-8233_87e5dcaf-13d8-46df-b4bf-b56723b2e77c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2013-04-10
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-8233-1 | 63629823301 | 90 TABLET in 1 BOTTLE (63629-8233-1) | 90 tablet | 2019-09-06 | 0000-00-00 | No | No | Current |
| 63629-8233-2 | 63629823302 | 30 TABLET in 1 BOTTLE (63629-8233-2) | 30 tablet | 2019-09-06 | 0000-00-00 | No | No | Current |