Package 68084-250-21

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 68084-250-21
Digits Only 6808425021
Product NDC 68084-250
Product ID 68084-250_37b3725e-fe41-d384-e063-6294a90a61da
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-250-21) / 1 TABLET in 1 BLISTER PACK (68084-250-11)

Marketing

Marketing Status
Marketed Since 2008-04-04
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": "37b3725e-fe41-d384-e063-6294a90a61da", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "314035"], "spl_set_id": ["0ac0cc44-3924-447d-9051-f84c44312380"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-250-21)  / 1 TABLET in 1 BLISTER PACK (68084-250-11)", "package_ndc": "68084-250-21", "marketing_start_date": "20080404"}], "brand_name": "Haloperidol", "product_id": "68084-250_37b3725e-fe41-d384-e063-6294a90a61da", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "68084-250", "generic_name": "Haloperidol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "20 mg/1"}], "application_number": "ANDA077580", "marketing_category": "ANDA", "marketing_start_date": "20080404", "listing_expiration_date": "20261231"}