Package 70518-1182-0

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 70518-1182-0
Digits Only 7051811820
Product NDC 70518-1182
Product ID 70518-1182_48c04dcd-77d9-3721-e063-6294a90ac815
Description

30 TABLET in 1 BLISTER PACK (70518-1182-0)

Marketing

Marketing Status
Marketed Since 2018-05-14
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": "48c04dcd-77d9-3721-e063-6294a90ac815", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310672"], "spl_set_id": ["1e396020-899d-4f51-b71a-4982c503ca4f"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1182-0)", "package_ndc": "70518-1182-0", "marketing_start_date": "20180514"}], "brand_name": "Haloperidol", "product_id": "70518-1182_48c04dcd-77d9-3721-e063-6294a90ac815", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "70518-1182", "generic_name": "Haloperidol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "5 mg/1"}], "application_number": "ANDA077580", "marketing_category": "ANDA", "marketing_start_date": "20180514", "listing_expiration_date": "20271231"}