Donepezil Hydrochloride 71335-0900
Product NDC
71335-0900- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 1, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA200292
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Donepezil Hydrochloride | 10 mg/1 |
Drug Class
Cholinesterase Inhibitor [EPC]Cholinesterase Inhibitors [MoA]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (71335-0900-1)
60 TABLET, FILM COATED in 1 BOTTLE (71335-0900-2)
90 TABLET, FILM COATED in 1 BOTTLE (71335-0900-3)