CHLORTHALIDONE
- Product NDC
- 71335-2223
- 11-digit product format
- 713352223
- Labeler code
- 71335
- Product ID
- 71335-2223_350a6448-3cf6-eb56-e063-6394a90a70c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA215587
- Marketing category
- ANDA
- Marketing start
- 2022-08-05
- 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 |
|---|
| 71335-2223-1 | 71335222301 | 30 TABLET in 1 BOTTLE (71335-2223-1) | 30 tablet | 2023-08-23 | No | No | Historical |
| 71335-2223-2 | 71335222302 | 90 TABLET in 1 BOTTLE (71335-2223-2) | 90 tablet | 2023-08-23 | No | No | Historical |
| 71335-2223-3 | 71335222303 | 60 TABLET in 1 BOTTLE (71335-2223-3) | 60 tablet | 2023-08-23 | No | No | Historical |
| 71335-2223-4 | 71335222304 | 8 TABLET in 1 BOTTLE (71335-2223-4) | 8 tablet | 2023-08-23 | No | No | Historical |
| 71335-2223-5 | 71335222305 | 100 TABLET in 1 BOTTLE (71335-2223-5) | 100 tablet | 2023-08-23 | No | No | Historical |