Package 58657-701-01

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 58657-701-01
Digits Only 5865770101
Product NDC 58657-701
Product ID 58657-701_38c21c0c-f6b3-adda-e063-6294a90a0ffd
Description

100 TABLET in 1 BOTTLE (58657-701-01)

Marketing

Marketing Status
Marketed Since 2019-11-25
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": "38c21c0c-f6b3-adda-e063-6294a90a0ffd", "openfda": {"nui": ["N0000180182"], "upc": ["0358657701109", "0358657702106", "0358657704018", "0358657700010", "0358657703011", "0358657702014", "0358657705015", "0358657700102", "0358657705107", "0358657905033", "0358657704100", "0358657701017", "0358657703103"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["87f8773b-bf89-4f7e-bff4-8cad117d5776"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (58657-701-01)", "package_ndc": "58657-701-01", "marketing_start_date": "20191125"}], "brand_name": "Haloperidol", "product_id": "58657-701_38c21c0c-f6b3-adda-e063-6294a90a0ffd", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "58657-701", "generic_name": "Haloperidol", "labeler_name": "Method Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "1 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20191125", "listing_expiration_date": "20261231"}