Hydrochlorothiazide
- Product NDC
- 72789-512
- 11-digit product format
- 727890512
- Labeler code
- 72789
- Product ID
- 72789-512_44086807-4be4-f324-e063-6394a90a0c49
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA083177
- Marketing category
- ANDA
- Marketing start
- 1973-01-12
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 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 | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0J48LPH2TH |
| Rxcui | 310798 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-512-30 | Hydrochlorothiazide | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 19 |
| 72789-512-60 | Hydrochlorothiazide | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 19 |
| 72789-512-90 | Hydrochlorothiazide | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 19 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-512-30 | 72789051230 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-512-30) | 30 tablet | 2025-06-06 | No | No | Current |
| 72789-512-60 | 72789051260 | 60 TABLET in 1 BOTTLE, PLASTIC (72789-512-60) | 60 tablet | 2025-10-29 | No | No | Current |
| 72789-512-90 | 72789051290 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-512-90) | 90 tablet | 2025-06-06 | No | No | Current |