Donepezil Hydrochloride
- Product NDC
- 57237-192
- 11-digit product format
- 572370192
- Labeler code
- 57237
- Product ID
- 57237-192_5fc06788-5c30-40fc-bab0-382173f99ed4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Citron Pharma LLC
- Application
- ANDA090056
- Marketing category
- ANDA
- Marketing start
- 2011-05-31
- Marketing end
- 0000-00-00
- Substance
- DONEPEZIL HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record