Donepezil Hydrochloride
- Product NDC
- 63629-5219
- 11-digit product format
- 636295219
- Labeler code
- 63629
- Product ID
- 63629-5219_6720ac23-fdba-41d5-984d-46c6867c10ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Donepezil Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090425
- Marketing category
- ANDA
- Marketing start
- 2011-05-31
- Marketing end
- 0000-00-00
- Substance
- DONEPEZIL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63629-5219-1 | 2021-06-01 | C162847 | 48780-1 | 9855e2a2-3bb5-60a7-e053-dbdaa90a05bd | d8e96754-8426-452f-83b8-c3528d820f25 |
| 63629-5219-2 | 2021-06-01 | C162847 | 48780-1 | 9855e2a2-3bb5-60a7-e053-dbdaa90a05bd | d8e96754-8426-452f-83b8-c3528d820f25 |
| 63629-5219-3 | 2021-06-01 | C162847 | 48780-1 | 9855e2a2-3bb5-60a7-e053-dbdaa90a05bd | d8e96754-8426-452f-83b8-c3528d820f25 |
| 63629-5219-1 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-3bb5-60a7-e053-dbdaa90a05bd | d8e96754-8426-452f-83b8-c3528d820f25 |
| 63629-5219-2 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-3bb5-60a7-e053-dbdaa90a05bd | d8e96754-8426-452f-83b8-c3528d820f25 |
| 63629-5219-3 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-3bb5-60a7-e053-dbdaa90a05bd | d8e96754-8426-452f-83b8-c3528d820f25 |