Package 72189-455-30

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 72189-455-30
Digits Only 7218945530
Product NDC 72189-455
Product ID 72189-455_2c4dbbad-3ed7-fec3-e063-6394a90a3b4d
Description

30 TABLET in 1 BOTTLE (72189-455-30)

Marketing

Marketing Status
Marketed Since 2023-03-30
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": "2c4dbbad-3ed7-fec3-e063-6394a90a3b4d", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349553"], "spl_set_id": ["f81d9b82-5879-3c0a-e053-6294a90ac23e"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-455-30)", "package_ndc": "72189-455-30", "marketing_start_date": "20230330"}], "brand_name": "Aripiprazole", "product_id": "72189-455_2c4dbbad-3ed7-fec3-e063-6394a90a3b4d", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-455", "generic_name": "Aripiprazole", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "20 mg/1"}], "application_number": "ANDA201519", "marketing_category": "ANDA", "marketing_start_date": "20230330", "listing_expiration_date": "20261231"}