Hydrochlorothiazide
- Product NDC
- 67296-1682
- 11-digit product format
- 672961682
- Labeler code
- 67296
- Product ID
- 67296-1682_b8df9dc5-96b4-e3c0-e053-2a95a90ab769
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2019-01-01
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 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 |
|---|
| 67296-1682-3 | Hydrochlorothiazide | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1682 | HYDROCHLOROTHIAZIDE TABLET [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 1 package rows | 20240806_89a94550-d005-6102-e053-2a95a90afe14.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 |
|---|
| 67296-1682-3 | 67296168203 | 30 TABLET in 1 BOTTLE (67296-1682-3) | 30 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |