CHLORTHALIDONE
- Product NDC
- 71335-2269
- 11-digit product format
- 713352269
- Labeler code
- 71335
- Product ID
- 71335-2269_8887b3a4-0310-4537-8427-1cc963160c15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211320
- Marketing category
- ANDA
- Marketing start
- 2021-03-31
- 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 |
|---|
| 71335-2269-1 | 71335226901 | 30 TABLET in 1 BOTTLE (71335-2269-1) | 30 tablet | 2023-11-30 | No | No | Historical |
| 71335-2269-2 | 71335226902 | 90 TABLET in 1 BOTTLE (71335-2269-2) | 90 tablet | 2023-11-30 | No | No | Historical |
| 71335-2269-3 | 71335226903 | 60 TABLET in 1 BOTTLE (71335-2269-3) | 60 tablet | 2023-11-30 | No | No | Historical |
| 71335-2269-4 | 71335226904 | 8 TABLET in 1 BOTTLE (71335-2269-4) | 8 tablet | 2023-11-30 | No | No | Historical |
| 71335-2269-5 | 71335226905 | 100 TABLET in 1 BOTTLE (71335-2269-5) | 100 tablet | 2023-11-30 | No | No | Historical |