Package 70518-3021-0

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 70518-3021-0
Digits Only 7051830210
Product NDC 70518-3021
Product ID 70518-3021_4af336d0-4aac-a0c8-e063-6394a90a4f51
Description

30 TABLET in 1 BLISTER PACK (70518-3021-0)

Marketing

Marketing Status
Marketed Since 2021-02-10
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": "4af336d0-4aac-a0c8-e063-6394a90a4f51", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["197754"], "spl_set_id": ["051f3c99-7d16-4185-a857-c90440e1b1c5"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3021-0)", "package_ndc": "70518-3021-0", "marketing_start_date": "20210210"}], "brand_name": "Haloperidol", "product_id": "70518-3021_4af336d0-4aac-a0c8-e063-6394a90a4f51", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "70518-3021", "generic_name": "Haloperidol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "20 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20210210", "listing_expiration_date": "20271231"}