Package 50268-087-12

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 50268-087-12
Digits Only 5026808712
Product NDC 50268-087
Description

20 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-087-12) / 1 TABLET in 1 BLISTER PACK (50268-087-11)

Marketing

Marketing Status
Marketed Since 2016-04-28
Brand aripiprazole
Generic aripiprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d49db38-3629-6bb9-e063-6294a90a4b4a", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["7df4c83e-13d8-25b1-57eb-08d26ba03565"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-087-12)  / 1 TABLET in 1 BLISTER PACK (50268-087-11)", "package_ndc": "50268-087-12", "marketing_start_date": "20160428"}], "brand_name": "Aripiprazole", "product_id": "50268-087_3d49db38-3629-6bb9-e063-6294a90a4b4a", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50268-087", "generic_name": "Aripiprazole", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA205064", "marketing_category": "ANDA", "marketing_start_date": "20160428", "listing_expiration_date": "20261231"}