Chlorthalidone
- Product NDC
- 68071-2037
- 11-digit product format
- 680712037
- Labeler code
- 68071
- Product ID
- 68071-2037_46e027f8-ce6a-3471-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA089286
- Marketing category
- ANDA
- Marketing start
- 2016-02-12
- 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