HYDROCHLOROTHIAZIDE
- Product NDC
- 68071-5284
- 11-digit product format
- 680715284
- Labeler code
- 68071
- Product ID
- 68071-5284_dfc93cb0-dd47-7d7e-e053-2a95a90a5ef1
- 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 |
|---|
| 68071-5284-1 | 68071528401 | 100 TABLET in 1 BOTTLE (68071-5284-1) | 100 tablet | 2020-06-18 | 0000-00-00 | No | No | Current |