Chlorthalidone
- Product NDC
- 68788-6852
- 11-digit product format
- 687886852
- Labeler code
- 68788
- Product ID
- 68788-6852_c3cdd532-8d5b-4b90-b7d5-e98b1527a705
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA089286
- Marketing category
- ANDA
- Marketing start
- 2016-12-12
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record