Package 51079-733-20

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 51079-733-20
Digits Only 5107973320
Product NDC 51079-733
Product ID 51079-733_3dd4fea4-d455-5a4d-e063-6394a90ab14c
Description

100 BLISTER PACK in 1 CARTON (51079-733-20) / 1 TABLET in 1 BLISTER PACK (51079-733-01)

Marketing

Marketing Status
Marketed Since 2004-02-01
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": "3dd4fea4-d455-5a4d-e063-6394a90ab14c", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["ad7d2f17-a4e8-4ebc-9baf-5983ac626782"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-733-20)  / 1 TABLET in 1 BLISTER PACK (51079-733-01)", "package_ndc": "51079-733-20", "marketing_start_date": "20040201"}], "brand_name": "Haloperidol", "product_id": "51079-733_3dd4fea4-d455-5a4d-e063-6394a90ab14c", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "51079-733", "generic_name": "haloperidol", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": ".5 mg/1"}], "application_number": "ANDA070278", "marketing_category": "ANDA", "marketing_start_date": "20040201", "listing_expiration_date": "20261231"}