Package 63629-9270-1
Brand: haloperidol
Generic: haloperidolPackage Facts
Identity
Package NDC
63629-9270-1
Digits Only
6362992701
Product NDC
63629-9270
Description
100 TABLET in 1 BOTTLE (63629-9270-1)
Marketing
Marketing Status
Brand
haloperidol
Generic
haloperidol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5389ec77-12c4-48f9-90ee-7e372c69c6c2", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310670"], "spl_set_id": ["88031df0-90bd-4444-9503-1b4612e3856b"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-9270-1)", "package_ndc": "63629-9270-1", "marketing_start_date": "20220418"}], "brand_name": "Haloperidol", "product_id": "63629-9270_5389ec77-12c4-48f9-90ee-7e372c69c6c2", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "63629-9270", "generic_name": "Haloperidol", "labeler_name": "Bryant Ranch Prepack", "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": "20191125", "listing_expiration_date": "20261231"}