donepezil hydrochloride
- Product NDC
- 63629-1117
- 11-digit product format
- 636291117
- Labeler code
- 63629
- Product ID
- 63629-1117_f77a7c2b-6644-4cb0-ab42-7cd5bc6ce288
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- donepezil hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203713
- Marketing category
- ANDA
- Marketing start
- 2016-12-05
- Marketing end
- 0000-00-00
- Substance
- DONEPEZIL HYDROCHLORIDE
- Active strength
- 23 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-1117 | DONEPEZIL HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 3 | Legacy NDC | 20240110_c7def1b5-ed4d-4eb8-b566-08dbab830cfb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1117-1 | 63629111701 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-1117-1) | 2020-07-30 | 0000-00-00 | No | No | Current |