Package 46708-260-10

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 46708-260-10
Digits Only 4670826010
Product NDC 46708-260
Description

30 TABLET, ORALLY DISINTEGRATING in 1 CARTON (46708-260-10)

Marketing

Marketing Status
Marketed Since 2015-05-21
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": "1ea06df8-17dc-46eb-921a-2b52d41ea622", "openfda": {"nui": ["N0000175430"], "upc": ["0346708261108", "0346708260101"], "unii": ["82VFR53I78"], "rxcui": ["643019", "643022"], "spl_set_id": ["4f1691a8-724e-430d-9bab-27b59ef9bd4e"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 CARTON (46708-260-10)", "package_ndc": "46708-260-10", "marketing_start_date": "20150521"}], "brand_name": "Aripiprazole", "product_id": "46708-260_1ea06df8-17dc-46eb-921a-2b52d41ea622", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "46708-260", "generic_name": "Aripiprazole", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "10 mg/1"}], "application_number": "ANDA202102", "marketing_category": "ANDA", "marketing_start_date": "20150521", "listing_expiration_date": "20261231"}