Chlorthalidone
- Product NDC
- 50090-7831
- 11-digit product format
- 500907831
- Labeler code
- 50090
- Product ID
- 50090-7831_4af0e626-dc1b-45e2-a773-e879d7190294
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA213412
- Marketing category
- ANDA
- Marketing start
- 2020-02-13
- Substance
- CHLORTHALIDONE
- Active strength
- 25 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 |
|---|
| 50090-7831-0 | 50090783100 | 90 TABLET in 1 BOTTLE (50090-7831-0) | 90 tablet | 2025-12-18 | No | No | Historical |