CHLORTHALIDONE
- Product NDC
- 70518-0740
- 11-digit product format
- 705180740
- Labeler code
- 70518
- Product ID
- 70518-0740_8e793739-6c87-a9a4-e053-2995a90a3386
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206904
- Marketing category
- ANDA
- Marketing start
- 2017-09-19
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record