Package 0904-6656-40

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 0904-6656-40
Digits Only 0904665640
Product NDC 0904-6656
Product ID 0904-6656_07e84436-8be5-4a0b-bcb8-5621edf984a9
Description

500 TABLET in 1 BOTTLE (0904-6656-40)

Marketing

Marketing Status
Marketed Since 2015-04-28
Brand aripiprazole
Generic aripiprazole
Sample Package No

Linked Drug Pages (1)

aripiprazole ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "07e84436-8be5-4a0b-bcb8-5621edf984a9", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["969c17aa-6abc-413c-8561-f1ad8fdde3e5"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (0904-6656-40)", "package_ndc": "0904-6656-40", "marketing_start_date": "20150428"}], "brand_name": "aripiprazole", "product_id": "0904-6656_07e84436-8be5-4a0b-bcb8-5621edf984a9", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-6656", "generic_name": "aripiprazole", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA201519", "marketing_category": "ANDA", "marketing_start_date": "20150428", "listing_expiration_date": "20261231"}