Hydrochlorothiazide
- Product NDC
- 63629-1219
- 11-digit product format
- 636291219
- Labeler code
- 63629
- Product ID
- 63629-1219_bcf88cbb-0746-4f47-a6f5-428618f38af9
- 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
- 2023-12-31
- 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 |
|---|
| 63629-1219 | HYDROCHLOROTHIAZIDE TABLET [BRYANT RANCH PREPACK] | 102 | Legacy NDC | 20230520_ff0270d7-e867-4cf9-9451-8545c73fa92b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1219-1 | 63629121901 | 1000 TABLET in 1 BOTTLE (63629-1219-1) | 1000 tablet | 2021-01-14 | 0000-00-00 | No | No | Current |