Chlorthalidone
- Product NDC
- 71335-2956
- 11-digit product format
- 713352956
- Labeler code
- 71335
- Product ID
- 71335-2956_d33219a3-f318-4f14-b455-4dcfb39d5497
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207222
- Marketing category
- ANDA
- Marketing start
- 2018-05-28
- 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 |
|---|
| 71335-2956-1 | 71335295601 | 100 TABLET in 1 BOTTLE (71335-2956-1) | 100 tablet | 2025-11-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ® Tablets | Bryant Ranch Prepack | 2025-11-11 | HUMAN PRESCRIPTION DRUG LABEL | 100 |