HYDROCHLOROTHIAZIDE
- Product NDC
- 70518-4466
- 11-digit product format
- 705184466
- Labeler code
- 70518
- Product ID
- 70518-4466_4149f0d8-1e41-f7f3-e063-6394a90a0d55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040702
- Marketing category
- ANDA
- Marketing start
- 2025-09-04
- 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 | 429503 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4466-0 | HYDROCHLOROTHIAZIDE | 30 in 1 BLISTER PACK | TABLET | 30 | | 2 |
| 70518-4466-1 | HYDROCHLOROTHIAZIDE | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4466-0 | 70518446600 | 30 TABLET in 1 BLISTER PACK (70518-4466-0) | 30 tablet | 2025-09-04 | No | No | Historical |
| 70518-4466-1 | 70518446601 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-4466-1) | 90 tablet | 2025-10-16 | No | No | Historical |