Hydrochlorothiazide
- Product NDC
- 68071-2462
- 11-digit product format
- 680712462
- Labeler code
- 68071
- Product ID
- 68071-2462_c5edeed7-47ee-2756-e053-2995a90ab0b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2013-04-18
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2462 | HYDROCHLOROTHIAZIDE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC | 20210630_c5ed8088-3a8b-dc72-e053-2995a90a4b09.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2462-3 | 68071246203 | 30 TABLET in 1 BOTTLE (68071-2462-3) | 30 tablet | 2021-06-29 | 0000-00-00 | No | No | Current |