Package 68071-3725-3

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 68071-3725-3
Digits Only 6807137253
Product NDC 68071-3725
Product ID 68071-3725_27877179-645e-dcc2-e063-6394a90aa66c
Description

30 TABLET in 1 BOTTLE (68071-3725-3)

Marketing

Marketing Status
Marketed Since 2024-11-22
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": "27877179-645e-dcc2-e063-6394a90aa66c", "openfda": {"nui": ["N0000175430"], "upc": ["0368071372533"], "unii": ["82VFR53I78"], "rxcui": ["602964"], "spl_set_id": ["27874fe2-3fd6-002d-e063-6294a90a4cd7"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3725-3)", "package_ndc": "68071-3725-3", "marketing_start_date": "20241122"}], "brand_name": "Aripiprazole", "product_id": "68071-3725_27877179-645e-dcc2-e063-6394a90aa66c", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3725", "generic_name": "Aripiprazole", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA207105", "marketing_category": "ANDA", "marketing_start_date": "20190227", "listing_expiration_date": "20261231"}