Hydrochlorothiazide
- Product NDC
- 68071-4807
- 11-digit product format
- 680714807
- Labeler code
- 68071
- Product ID
- 68071-4807_bb8f6d05-d6c1-23e1-e053-2a95a90a6496
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040907
- Marketing category
- ANDA
- Marketing start
- 2009-07-02
- 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
- 2022-12-31
- 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 |
|---|
| 68071-4807-3 | 68071480703 | 30 TABLET in 1 BOTTLE (68071-4807-3) | 30 tablet | 2019-03-20 | 0000-00-00 | No | No | Current |