CHLORTHALIDONE
- Product NDC
- 71610-472
- 11-digit product format
- 716100472
- Labeler code
- 71610
- Product ID
- 71610-472_e74a8605-c417-45b6-a098-5046a5e3c446
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA206904
- Marketing category
- ANDA
- Marketing start
- 2017-05-17
- 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 |
|---|
| 71610-472-30 | 71610047230 | 30 TABLET in 1 BOTTLE, PLASTIC (71610-472-30) | 30 tablet | 2020-10-09 | No | No | Historical |
| 71610-472-45 | 71610047245 | 45 TABLET in 1 BOTTLE, PLASTIC (71610-472-45) | 45 tablet | 2020-10-09 | No | No | Historical |
| 71610-472-60 | 71610047260 | 90 TABLET in 1 BOTTLE, PLASTIC (71610-472-60) | 90 tablet | 2020-10-09 | No | No | Historical |