Donepezil Hydrochloride
- Product NDC
- 55154-6891
- 11-digit product format
- 551546891
- Labeler code
- 55154
- Product ID
- 55154-6891_d454ce92-05d6-403d-a264-b7f52f8b1153
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA201724
- Marketing category
- ANDA
- Marketing start
- 2014-06-15
- Marketing end
- 0000-00-00
- Substance
- DONEPEZIL HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record