HYDROCHLOROTHIAZIDE
- Product NDC
- 67296-1423
- 11-digit product format
- 672961423
- Labeler code
- 67296
- Product ID
- 67296-1423_bb68cdbe-eafa-92e3-e053-2995a90ae210
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1423-3 | HYDROCHLOROTHIAZIDE | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1423 | HYDROCHLOROTHIAZIDE TABLET [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20240808_bb68d143-3af4-7b9e-e053-2995a90a140f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1423-3 | 67296142303 | 30 TABLET in 1 BOTTLE (67296-1423-3) | 30 tablet | 2021-02-15 | 0000-00-00 | No | No | Current |