Donepezil Hydrochloride 62756-0194
Product NDC
62756-0194- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 17, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA204293
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Donepezil Hydrochloride | 23 mg/1 |
Drug Class
Cholinesterase Inhibitor [EPC]Cholinesterase Inhibitors [MoA]
Packaging Options(3)
1000 TABLET, FILM COATED in 1 BOTTLE (62756-194-18)
90 TABLET, FILM COATED in 1 BOTTLE (62756-194-81)
30 TABLET, FILM COATED in 1 BOTTLE (62756-194-83)