Chlorthalidone
- Product NDC
- 63629-8762
- 11-digit product format
- 636298762
- Labeler code
- 63629
- Product ID
- 63629-8762_9c48d444-00d6-4ec7-af5c-f205dd4d1870
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213412
- Marketing category
- ANDA
- Marketing start
- 2020-02-13
- 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 |
|---|
| 63629-8762-1 | 63629876201 | 100 TABLET in 1 BOTTLE (63629-8762-1) | 100 tablet | 2020-02-13 | No | No | Historical |