Donepezil
- Product NDC
- 68071-4613
- 11-digit product format
- 680714613
- Labeler code
- 68071
- Product ID
- 68071-4613_bbf24103-51d2-3f02-e053-2a95a90a1feb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4613-9 | 68071461309 | 90 TABLET in 1 BOTTLE (68071-4613-9) | 90 tablet | 2018-10-24 | 0000-00-00 | No | No | Current |