donepezil hydrochloride
- Product NDC
- 50090-1287
- 11-digit product format
- 500901287
- Labeler code
- 50090
- Product ID
- 50090-1287_33c32fae-933d-462b-a770-0434051d4114
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- donepezil hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA200292
- Marketing category
- ANDA
- Marketing start
- 2011-11-01
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1287-0 | 50090128700 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-1287-0) | 2014-11-28 | 0000-00-00 | No | No | Current |