Donepezil Hyrochloride
- Product NDC
- 62980-504
- 11-digit product format
- 629800504
- Labeler code
- 62980
- Product ID
- 62980-504_ee5bc05c-0927-449f-936a-e4c533b895d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL; ORAL; ORAL; ORAL; ORAL; ORAL; ORAL
- Labeler
- Vivimed Labs Limited
- Application
- ANDA090551
- Marketing category
- ANDA
- Marketing start
- 2015-07-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record