Package 71335-2937-1

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 71335-2937-1
Digits Only 7133529371
Product NDC 71335-2937
Product ID 71335-2937_01dbf8b5-6b02-43f2-bc9c-eee7c8da6cb1
Description

30 TABLET in 1 BOTTLE (71335-2937-1)

Marketing

Marketing Status
Marketed Since 2025-10-28
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": "01dbf8b5-6b02-43f2-bc9c-eee7c8da6cb1", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["314034"], "spl_set_id": ["ea01b32e-5abe-455d-8813-cef101fa53f1"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2937-1)", "package_ndc": "71335-2937-1", "marketing_start_date": "20251028"}], "brand_name": "Haloperidol", "product_id": "71335-2937_01dbf8b5-6b02-43f2-bc9c-eee7c8da6cb1", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "71335-2937", "generic_name": "Haloperidol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "2 mg/1"}], "application_number": "ANDA218789", "marketing_category": "ANDA", "marketing_start_date": "20240419", "listing_expiration_date": "20261231"}