Chlorthalidone
- Product NDC
- 72162-2134
- 11-digit product format
- 721622134
- Labeler code
- 72162
- Product ID
- 72162-2134_deceb103-0c69-4dea-8c7b-92f50e8b872b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212875
- 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 |
|---|
| 72162-2134-1 | 72162213401 | 100 TABLET in 1 BOTTLE (72162-2134-1) | 100 tablet | 2023-09-20 | No | No | Historical |
| 72162-2134-3 | 72162213403 | 30 TABLET in 1 BOTTLE (72162-2134-3) | 30 tablet | 2023-09-20 | No | No | Historical |
| 72162-2134-6 | 72162213406 | 60 TABLET in 1 BOTTLE (72162-2134-6) | 60 tablet | 2023-09-20 | No | No | Historical |