DONEPEZIL HYDROCHLORIDE
- Product NDC
- 0179-0208
- 11-digit product format
- 001790208
- Labeler code
- 0179
- Product ID
- 0179-0208_7bab8864-f466-0c17-e053-2a91aa0a5bc5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DONEPEZIL HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA090768
- Marketing category
- ANDA
- Marketing start
- 2016-06-29
- Marketing end
- 2020-02-29
- Substance
- DONEPEZIL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record