Chlorthalidone
- Product NDC
- 70518-2552
- 11-digit product format
- 705182552
- Labeler code
- 70518
- Product ID
- 70518-2552_ca00dfa7-458e-1721-e053-2a95a90a7c2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211063
- Marketing category
- ANDA
- Marketing start
- 2020-01-22
- Marketing end
- 0000-00-00
- Substance
- CHLORTHALIDONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Thiazide-like Diuretic [EPC],Increased Diuresis [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-2552-0 | 70518255200 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2552-0) | 90 tablet | 2020-01-22 | 0000-00-00 | No | No | Current |