Hydrochlorothiazide
- Product NDC
- 70934-789
- 11-digit product format
- 709340789
- Labeler code
- 70934
- Product ID
- 70934-789_c181aebd-b0a9-d302-e053-2a95a90a8e52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA040907
- Marketing category
- ANDA
- Marketing start
- 2020-08-18
- 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 |
|---|
| 70934-789-30 | 70934078930 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-789-30) | 30 tablet | 2020-08-18 | 0000-00-00 | No | No | Current |
| 70934-789-90 | 70934078990 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-789-90) | 90 tablet | 2021-05-03 | 0000-00-00 | No | No | Current |