HYDROCHLOROTHIAZIDE
- Product NDC
- 72189-263
- 11-digit product format
- 721890263
- Labeler code
- 72189
- Product ID
- 72189-263_2c29005f-2597-e87a-e063-6294a90a2fc3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA202556
- Marketing category
- ANDA
- Marketing start
- 2021-09-13
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- HYDROCHLOROTHIAZIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCHLOROTHIAZIDE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0J48LPH2TH |
| Rxcui | 197770 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-263-90 | HYDROCHLOROTHIAZIDE | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-263 | HYDROCHLOROTHIAZIDE TABLET [DIRECT RX] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250121_cbe5e01e-67ca-f8a2-e053-2995a90a0d15.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 |
|---|
| 72189-263-90 | 72189026390 | 90 TABLET in 1 BOTTLE (72189-263-90) | 90 tablet | 2021-09-13 | 0000-00-00 | No | No | Current |