CHLORTHALIDONE
- Product NDC
- 55801-145
- 11-digit product format
- 558010145
- Labeler code
- 55801
- Product ID
- 55801-145_0b2ef41b-bbab-432a-b7fa-dd4a87050d46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Appco Pharma LLC
- Application
- ANDA210742
- Marketing category
- ANDA
- Marketing start
- 2018-10-22
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record