Donepezil
- Product NDC
- 68788-7632
- 11-digit product format
- 687887632
- Labeler code
- 68788
- Product ID
- 68788-7632_4fb76910-c9c1-4c0a-8cba-511d3e1e5d55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA203034
- Marketing category
- ANDA
- Marketing start
- 2020-03-06
- 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
- 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 |
|---|
| 68788-7632-3 | 68788763203 | 30 TABLET in 1 BOTTLE (68788-7632-3) | 30 tablet | 2020-03-06 | 0000-00-00 | No | No | Current |
| 68788-7632-6 | 68788763206 | 60 TABLET in 1 BOTTLE (68788-7632-6) | 60 tablet | 2020-03-06 | 0000-00-00 | No | No | Current |
| 68788-7632-9 | 68788763209 | 90 TABLET in 1 BOTTLE (68788-7632-9) | 90 tablet | 2020-03-06 | 0000-00-00 | No | No | Current |