Package 68071-3848-3

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 68071-3848-3
Digits Only 6807138483
Product NDC 68071-3848
Description

30 TABLET in 1 BOTTLE (68071-3848-3)

Marketing

Marketing Status
Marketed Since 2025-08-22
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": "3cf72865-97f2-2fea-e063-6394a90ab9cb", "openfda": {"nui": ["N0000175430"], "upc": ["0368071384833"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["3cf72cc6-ae43-bfd5-e063-6294a90a18b0"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3848-3)", "package_ndc": "68071-3848-3", "marketing_start_date": "20250822"}], "brand_name": "Aripiprazole", "product_id": "68071-3848_3cf72865-97f2-2fea-e063-6394a90ab9cb", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3848", "generic_name": "Aripiprazole", "labeler_name": "NuCare 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"}