Package 72789-462-14

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 72789-462-14
Digits Only 7278946214
Product NDC 72789-462
Description

14 TABLET in 1 BOTTLE, PLASTIC (72789-462-14)

Marketing

Marketing Status
Marketed Since 2024-12-23
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": "41252b86-af95-c707-e063-6394a90af48d", "openfda": {"nui": ["N0000175430"], "upc": ["0372789462141"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["0cf6655e-d59a-4ebd-9698-195cad2adbd5"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (72789-462-14)", "package_ndc": "72789-462-14", "marketing_start_date": "20241223"}], "brand_name": "Aripiprazole", "product_id": "72789-462_41252b86-af95-c707-e063-6394a90af48d", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72789-462", "generic_name": "Aripiprazole", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20150428", "listing_expiration_date": "20261231"}