Package 72189-466-30

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 72189-466-30
Digits Only 7218946630
Product NDC 72189-466
Product ID 72189-466_2c4def88-252d-7c8b-e063-6294a90aeb94
Description

30 TABLET in 1 BOTTLE (72189-466-30)

Marketing

Marketing Status
Marketed Since 2023-05-03
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": "2c4def88-252d-7c8b-e063-6294a90aeb94", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["602964"], "spl_set_id": ["facdb9a9-612f-e59a-e053-6394a90a1fa7"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-466-30)", "package_ndc": "72189-466-30", "marketing_start_date": "20230503"}], "brand_name": "Aripiprazole", "product_id": "72189-466_2c4def88-252d-7c8b-e063-6294a90aeb94", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-466", "generic_name": "Aripiprazole", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA207105", "marketing_category": "ANDA", "marketing_start_date": "20230503", "listing_expiration_date": "20261231"}