Chlorthalidone
- Product NDC
- 70518-1376
- 11-digit product format
- 705181376
- Labeler code
- 70518
- Product ID
- 70518-1376_d93fb144-ced2-9ca5-e053-2a95a90a4ec8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207222
- Marketing category
- ANDA
- Marketing start
- 2018-08-15
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1376-0 | 70518137600 | 30 TABLET in 1 BLISTER PACK (70518-1376-0) | 30 tablet | 2018-08-15 | 0000-00-00 | No | No | Current |
| 70518-1376-2 | 70518137602 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1376-2) | 90 tablet | 2021-05-12 | 0000-00-00 | No | No | Current |