Package 70518-2687-0

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 70518-2687-0
Digits Only 7051826870
Product NDC 70518-2687
Product ID 70518-2687_4a7e0f6e-afb4-53fc-e063-6294a90a398b
Description

30 TABLET in 1 BLISTER PACK (70518-2687-0)

Marketing

Marketing Status
Marketed Since 2020-04-13
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": "4a7e0f6e-afb4-53fc-e063-6294a90a398b", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310670"], "spl_set_id": ["b5a6c54c-fb70-4132-90ae-7d75b5e9c9de"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2687-0)", "package_ndc": "70518-2687-0", "marketing_start_date": "20200413"}], "brand_name": "Haloperidol", "product_id": "70518-2687_4a7e0f6e-afb4-53fc-e063-6294a90a398b", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "70518-2687", "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": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20200413", "listing_expiration_date": "20271231"}