CHLORTHALIDONE
- Product NDC
- 63629-4446
- 11-digit product format
- 636294446
- Labeler code
- 63629
- Product ID
- 63629-4446_5ee6b004-4e5c-4f15-bbf1-3db44d7063a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA215587
- Marketing category
- ANDA
- Marketing start
- 2022-08-05
- Substance
- CHLORTHALIDONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| Q0MQD1073Q | CHLORTHALIDONE | 77-36-1 | CHLORTHALIDONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-4446-1 | 63629444601 | 90 TABLET in 1 BOTTLE (63629-4446-1) | 90 tablet | 2024-08-22 | No | No | Historical |