Donepezil Hydrochloride 55111-0357
Product NDC
55111-0357- Manufacturer
- Dr. Reddys Laboratories Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 31, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA201001
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Donepezil Hydrochloride | 10 mg/1 |
Drug Class
Cholinesterase Inhibitor [EPC]Cholinesterase Inhibitors [MoA]
Packaging Options(5)
500 TABLET, FILM COATED in 1 BOTTLE (55111-357-05)
1000 TABLET, FILM COATED in 1 BOTTLE (55111-357-10)
30 TABLET, FILM COATED in 1 BOTTLE (55111-357-30)
10 BLISTER PACK in 1 CARTON (55111-357-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-357-79)
90 TABLET, FILM COATED in 1 BOTTLE (55111-357-90)