Package 0093-2401-01

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 0093-2401-01
Digits Only 0093240101
Product NDC 0093-2401
Product ID 0093-2401_0ed011f2-0881-4bd1-ab62-1cd84a48ed52
Description

100 TABLET, FILM COATED in 1 BOTTLE (0093-2401-01)

Marketing

Marketing Status
Marketed Since 2020-10-08
Brand hydroxychloroquine sulfate
Generic hydroxychloroquine sulfate
Sample Package No

Linked Drug Pages (1)

Hydroxychloroquine Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0ed011f2-0881-4bd1-ab62-1cd84a48ed52", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["5f3e49b2-dc11-40a9-b366-c88e36a471e5"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-2401-01)", "package_ndc": "0093-2401-01", "marketing_start_date": "20201008"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "0093-2401_0ed011f2-0881-4bd1-ab62-1cd84a48ed52", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "0093-2401", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine Sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040081", "marketing_category": "ANDA", "marketing_start_date": "20201008", "listing_expiration_date": "20261231"}