Donepezil Hydrochloride
- Product NDC
- 63629-8050
- 11-digit product format
- 636298050
- Labeler code
- 63629
- Product ID
- 63629-8050_12a8f69c-6537-4131-9f63-6776e81b21d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201146
- Marketing category
- ANDA
- Marketing start
- 2012-08-17
- Marketing end
- 0000-00-00
- Substance
- DONEPEZIL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8050-1 | 63629805001 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8050-1) | 2019-07-15 | 0000-00-00 | No | No | Current |