Hydrochlorothiazide
- Product NDC
- 68071-2456
- 11-digit product format
- 680712456
- Labeler code
- 68071
- Product ID
- 68071-2456_c55fd54a-b01b-44ec-e053-2a95a90a82e7
- 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 |
|---|
| 68071-2456 | HYDROCHLOROTHIAZIDE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC | 20210623_c55fd90f-1e34-557d-e053-2a95a90ab2f5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2456-1 | 68071245601 | 100 TABLET in 1 BOTTLE (68071-2456-1) | 100 tablet | 2021-06-22 | 0000-00-00 | No | No | Current |