Hydrochlorothiazide
- Product NDC
- 64725-0047
- 11-digit product format
- 647250047
- Labeler code
- 64725
- Product ID
- 64725-0047_c2dad462-8302-427f-91e3-e1c08a9b2a34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA040807
- Marketing category
- ANDA
- Marketing start
- 2010-08-20
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64725-0047-1 | Hydrochlorothiazide | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-0047 | HYDROCHLOROTHIAZIDE TABLET [TYA PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20140901_4ea10b58-88d0-4d7f-ba20-bec824d1d2bd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-0047-1 | 64725004701 | 100 in 1 BOTTLE | Historical |