Package 70518-2736-0

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 70518-2736-0
Digits Only 7051827360
Product NDC 70518-2736
Description

30 TABLET in 1 BLISTER PACK (70518-2736-0)

Marketing

Marketing Status
Marketed Since 2020-05-12
Brand aripiprazole
Generic aripiprazole
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a8cee22-16db-98ca-e063-6294a90aa648", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["602964"], "spl_set_id": ["2bc00231-c2e7-4b9d-93a1-fb796fd8d591"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2736-0)", "package_ndc": "70518-2736-0", "marketing_start_date": "20200512"}], "brand_name": "Aripiprazole", "product_id": "70518-2736_4a8cee22-16db-98ca-e063-6294a90aa648", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2736", "generic_name": "Aripiprazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA206174", "marketing_category": "ANDA", "marketing_start_date": "20200512", "listing_expiration_date": "20271231"}