Package 70518-2680-0

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 70518-2680-0
Digits Only 7051826800
Product NDC 70518-2680
Product ID 70518-2680_4a7dc8e9-6ded-7c68-e063-6394a90a8e62
Description

30 TABLET in 1 BLISTER PACK (70518-2680-0)

Marketing

Marketing Status
Marketed Since 2020-04-08
Brand haloperidol
Generic haloperidol
Sample Package No

Linked Drug Pages (1)

Haloperidol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a7dc8e9-6ded-7c68-e063-6394a90a8e62", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["314034"], "spl_set_id": ["eb69959d-5967-41ac-a222-ff4416869dfc"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2680-0)", "package_ndc": "70518-2680-0", "marketing_start_date": "20200408"}], "brand_name": "Haloperidol", "product_id": "70518-2680_4a7dc8e9-6ded-7c68-e063-6394a90a8e62", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "70518-2680", "generic_name": "Haloperidol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "2 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20200408", "listing_expiration_date": "20271231"}