Package 72189-456-30

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 72189-456-30
Digits Only 7218945630
Product NDC 72189-456
Product ID 72189-456_2c4dbb36-483f-f211-e063-6294a90ad364
Description

30 TABLET in 1 BOTTLE (72189-456-30)

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": "2c4dbb36-483f-f211-e063-6294a90ad364", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["f823bc23-27f3-2397-e053-6294a90a365a"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-456-30)", "package_ndc": "72189-456-30", "marketing_start_date": "20230330"}], "brand_name": "Aripiprazole", "product_id": "72189-456_2c4dbb36-483f-f211-e063-6294a90ad364", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-456", "generic_name": "Aripiprazole", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA205064", "marketing_category": "ANDA", "marketing_start_date": "20230330", "listing_expiration_date": "20261231"}