Hydrochlorothiazide
- Product NDC
- 68071-4176
- 11-digit product format
- 680714176
- Labeler code
- 68071
- Product ID
- 68071-4176_bb64231a-3b27-3c15-e053-2a95a90ad079
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- NDA020504
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1996-12-27
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4176-3 | 68071417603 | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (68071-4176-3) | 2017-12-06 | 0000-00-00 | No | No | Current |
| 68071-4176-6 | 68071417606 | 60 CAPSULE, GELATIN COATED in 1 BOTTLE (68071-4176-6) | 2017-12-06 | 0000-00-00 | No | No | Current |
| 68071-4176-9 | 68071417609 | 90 CAPSULE, GELATIN COATED in 1 BOTTLE (68071-4176-9) | 2017-12-06 | 0000-00-00 | No | No | Current |