Donepezil Hydrochloride
- Product NDC
- 0781-5274
- 11-digit product format
- 007815274
- Labeler code
- 0781
- Product ID
- 0781-5274_a878e36d-bdf5-43ff-8f8a-b5a1d16f1e30
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA090290
- 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
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record