Donepezil
- Product NDC
- 71335-0792
- 11-digit product format
- 713350792
- Labeler code
- 71335
- Product ID
- 71335-0792_f118d721-590a-4fbd-8433-b1f33c901cb1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203034
- Marketing category
- ANDA
- Marketing start
- 2015-02-02
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0792-1 | 71335079201 | 30 TABLET in 1 BOTTLE (71335-0792-1) | 30 tablet | 2018-05-01 | 0000-00-00 | No | No | Current |
| 71335-0792-2 | 71335079202 | 60 TABLET in 1 BOTTLE (71335-0792-2) | 60 tablet | 2018-05-01 | 0000-00-00 | No | No | Current |
| 71335-0792-3 | 71335079203 | 90 TABLET in 1 BOTTLE (71335-0792-3) | 90 tablet | 2018-05-01 | 0000-00-00 | No | No | Current |