Hydrochlorothiazide
- Product NDC
- 64725-0045
- 11-digit product format
- 647250045
- Labeler code
- 64725
- Product ID
- 64725-0045_fefc0b73-ba82-4ff3-b3ac-75860885cb45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA079237
- Marketing category
- ANDA
- Marketing start
- 2010-12-10
- 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
- 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 |
|---|
| 64725-0045-1 | Hydrochlorothiazide | 100 in 1 BOTTLE | CAPSULE | 100 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-0045 | HYDROCHLOROTHIAZIDE CAPSULE [TYA PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20141027_999116d1-7e33-4b7c-adef-39f067b40192.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-0045-1 | 64725004501 | 100 in 1 BOTTLE | Historical |