Hydrochlorothiazide
- Product NDC
- 68788-9965
- 11-digit product format
- 687889965
- Labeler code
- 68788
- Product ID
- 68788-9965_921ba904-2208-4493-b650-c016ed5485b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA040907
- Marketing category
- ANDA
- Marketing start
- 2015-05-05
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-9965-0 | 68788996500 | 100 TABLET in 1 BOTTLE (68788-9965-0) | 100 tablet | 2015-05-05 | 0000-00-00 | No | No | Current |
| 68788-9965-1 | 68788996501 | 15 TABLET in 1 BOTTLE (68788-9965-1) | 15 tablet | 2015-05-05 | 0000-00-00 | No | No | Current |
| 68788-9965-3 | 68788996503 | 30 TABLET in 1 BOTTLE (68788-9965-3) | 30 tablet | 2015-05-05 | 0000-00-00 | No | No | Current |
| 68788-9965-6 | 68788996506 | 60 TABLET in 1 BOTTLE (68788-9965-6) | 60 tablet | 2015-05-05 | 0000-00-00 | No | No | Current |
| 68788-9965-9 | 68788996509 | 90 TABLET in 1 BOTTLE (68788-9965-9) | 90 tablet | 2015-05-05 | 0000-00-00 | No | No | Current |