HYDROCHLOROTHIAZIDE
- Product NDC
- 68071-5266
- 11-digit product format
- 680715266
- Labeler code
- 68071
- Product ID
- 68071-5266_d771c3c1-7088-12af-e053-2995a90ad8fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare PHarmaceuticals,Inc.
- Application
- ANDA085182
- Marketing category
- ANDA
- Marketing start
- 2015-01-15
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5266-3 | 68071526603 | 30 TABLET in 1 BOTTLE (68071-5266-3) | 30 tablet | 2020-06-03 | 0000-00-00 | No | No | Current |