Donepezil Hydrochloride
- Product NDC
- 70518-0802
- 11-digit product format
- 705180802
- Labeler code
- 70518
- Product ID
- 70518-0802_8e675d87-f763-77d3-e053-2995a90a3628
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090686
- Marketing category
- ANDA
- Marketing start
- 2017-10-20
- 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