Donepezil Hydrochloride 50228-0139
Product NDC
50228-0139- Manufacturer
- Sciegen Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 29, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA203907
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Donepezil Hydrochloride | 5 mg/1 |
Drug Class
Cholinesterase Inhibitor [EPC]Cholinesterase Inhibitors [MoA]
Packaging Options(2)
1000 TABLET, FILM COATED in 1 BOTTLE (50228-139-10)
30 TABLET, FILM COATED in 1 BOTTLE (50228-139-30)