Package 68071-3906-4

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 68071-3906-4
Digits Only 6807139064
Product NDC 68071-3906
Description

14 TABLET in 1 BOTTLE (68071-3906-4)

Marketing

Marketing Status
Marketed Since 2025-10-16
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": "414b8086-6336-5388-e063-6294a90a9dbd", "openfda": {"nui": ["N0000175430"], "upc": ["0368071390643"], "unii": ["82VFR53I78"], "rxcui": ["349545"], "spl_set_id": ["414b7fd2-6a63-af39-e063-6394a90a00b8"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (68071-3906-4)", "package_ndc": "68071-3906-4", "marketing_start_date": "20251016"}], "brand_name": "Aripiprazole", "product_id": "68071-3906_414b8086-6336-5388-e063-6294a90a9dbd", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3906", "generic_name": "Aripiprazole", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "10 mg/1"}], "application_number": "ANDA205064", "marketing_category": "ANDA", "marketing_start_date": "20201001", "listing_expiration_date": "20261231"}