Chlorthalidone
- Product NDC
- 72189-507
- 11-digit product format
- 721890507
- Labeler code
- 72189
- Product ID
- 72189-507_2c4e39ee-1b2e-61c5-e063-6394a90aeef5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA214129
- Marketing category
- ANDA
- Marketing start
- 2023-08-17
- 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 |
|---|
| 72189-507-60 | 72189050760 | 60 TABLET in 1 BOTTLE (72189-507-60) | 60 tablet | 2023-08-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Chlorthalidone | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 3 |