Donepezil Hydrochloride 16571-0778
Product NDC
16571-0778- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 31, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA090056
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Donepezil Hydrochloride | 5 mg/1 |
Drug Class
Cholinesterase Inhibitor [EPC]Cholinesterase Inhibitors [MoA]
Packaging Options(4)
30 TABLET, FILM COATED in 1 BOTTLE (16571-778-03)
90 TABLET, FILM COATED in 1 BOTTLE (16571-778-09)
1000 TABLET, FILM COATED in 1 BOTTLE (16571-778-10)
500 TABLET, FILM COATED in 1 BOTTLE (16571-778-50)