CHLORTHALIDONE
- Product NDC
- 70518-2690
- 11-digit product format
- 705182690
- Labeler code
- 70518
- Product ID
- 70518-2690_dc8c6044-e831-da38-e053-2a95a90a0bce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210742
- Marketing category
- ANDA
- Marketing start
- 2020-04-14
- Marketing end
- 0000-00-00
- Substance
- CHLORTHALIDONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2690-0 | 70518269000 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2690-0) | 90 tablet | 2020-04-14 | 0000-00-00 | No | No | Current |