Package 50090-3537-0

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-3537-0
Digits Only 5009035370
Product NDC 50090-3537
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-3537-0)

Marketing

Marketing Status
Marketed Since 2018-08-15
Brand donepezil hydrochloride
Generic donepezil hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "88e8acb5-251c-442e-bd88-ea7cd0416c6e", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["5d46ef3c-0dee-4389-a2d5-997ea8342817"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-3537-0)", "package_ndc": "50090-3537-0", "marketing_start_date": "20180815"}], "brand_name": "donepezil hydrochloride", "product_id": "50090-3537_88e8acb5-251c-442e-bd88-ea7cd0416c6e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "50090-3537", "generic_name": "donepezil hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA200292", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}