Hydrochlorothiazide
- Product NDC
- 68645-341
- 11-digit product format
- 686450341
- Labeler code
- 68645
- Product ID
- 68645-341_1ca96cd5-8cfc-4491-8722-9c4a3f45fedc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2002-03-29
- 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
- 2019-12-31
- 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 |
|---|
| 68645-341-54 | Hydrochlorothiazide | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68645-341 | HYDROCHLOROTHIAZIDE TABLET [LEGACY PHARMACEUTICAL PACKAGING] | 1 | Legacy NDC, 1 package rows | 20120120_6d7e3b52-e26e-4e62-aa2e-31c87a6cd5bd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68645-341-54 | 68645034154 | 30 in 1 BOTTLE, PLASTIC | Historical |