Package 70518-4285-0

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 70518-4285-0
Digits Only 7051842850
Product NDC 70518-4285
Product ID 70518-4285_401b5d09-1bca-e6e0-e063-6294a90a2a0a
Description

30 TABLET in 1 BLISTER PACK (70518-4285-0)

Marketing

Marketing Status
Marketed Since 2025-02-11
Brand haloperidol
Generic haloperidol
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "401b5d09-1bca-e6e0-e063-6294a90a2a0a", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310672"], "spl_set_id": ["a0751f2e-05ab-4ba9-9bae-7b791bf1a621"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4285-0)", "package_ndc": "70518-4285-0", "marketing_start_date": "20250211"}], "brand_name": "Haloperidol", "product_id": "70518-4285_401b5d09-1bca-e6e0-e063-6294a90a2a0a", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "70518-4285", "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": "ANDA216918", "marketing_category": "ANDA", "marketing_start_date": "20250211", "listing_expiration_date": "20261231"}