Hydrochlorothiazide
- Product NDC
- 0172-3444
- 11-digit product format
- 001723444
- Labeler code
- 0172
- Product ID
- 0172-3444_6659686c-94ec-408c-b0bb-c78528aaa6c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA083177
- Marketing category
- ANDA
- Marketing start
- 2025-06-03
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 12.5 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 | 12.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0J48LPH2TH |
| Rxcui | 197770, 310798, 429503 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0172-3444-60 | Hydrochlorothiazide | 100 in 1 BOTTLE | TABLET | 100 | | 18 |
| 0172-3444-80 | Hydrochlorothiazide | 1000 in 1 BOTTLE | TABLET | 1000 | | 18 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0172-3444-60 | 00172344460 | 100 TABLET in 1 BOTTLE (0172-3444-60) | 100 tablet | 2025-09-09 | No | No | Current |
| 0172-3444-80 | 00172344480 | 1000 TABLET in 1 BOTTLE (0172-3444-80) | 1000 tablet | 2025-06-03 | No | No | Current |