Donepezil Hydrochloride 65862-0325
Product NDC
65862-0325- Manufacturer
- Aurobindo Pharma Limited
- 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(6)
100 TABLET, FILM COATED in 1 BOTTLE (65862-325-01)
500 TABLET, FILM COATED in 1 BOTTLE (65862-325-05)
10 BLISTER PACK in 1 CARTON (65862-325-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
30 TABLET, FILM COATED in 1 BOTTLE (65862-325-30)
90 TABLET, FILM COATED in 1 BOTTLE (65862-325-90)
1000 TABLET, FILM COATED in 1 BOTTLE (65862-325-99)