Hydrochlorothiazide
- Product NDC
- 63629-8991
- 11-digit product format
- 636298991
- Labeler code
- 63629
- Product ID
- 63629-8991_677b6fad-d4b9-4111-9a69-0720a10863c1
- 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
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8991 | HYDROCHLOROTHIAZIDE TABLET [BRYANT RANCH PREPACK] | 100 | Legacy NDC | 20211214_589c2ab2-46a8-4b99-94e2-38197ac881a3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8991-1 | 63629899101 | 30 TABLET in 1 BOTTLE, PLASTIC (63629-8991-1) | 30 tablet | 2021-12-07 | 0000-00-00 | No | No | Current |
| 63629-8991-2 | 63629899102 | 60 TABLET in 1 BOTTLE, PLASTIC (63629-8991-2) | 60 tablet | 2021-12-07 | 0000-00-00 | No | No | Current |
| 63629-8991-3 | 63629899103 | 90 TABLET in 1 BOTTLE, PLASTIC (63629-8991-3) | 90 tablet | 2021-12-07 | 0000-00-00 | No | No | Current |