Package 71335-2813-1

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 71335-2813-1
Digits Only 7133528131
Product NDC 71335-2813
Product ID 71335-2813_48df785b-43a2-49b6-8a5f-0bf9fbffa272
Description

100 TABLET in 1 BOTTLE (71335-2813-1)

Marketing

Marketing Status
Marketed Since 2025-10-02
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": "48df785b-43a2-49b6-8a5f-0bf9fbffa272", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["f95cfc03-5023-44b3-8994-25afac18b734"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2813-1)", "package_ndc": "71335-2813-1", "marketing_start_date": "20251002"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "71335-2813_48df785b-43a2-49b6-8a5f-0bf9fbffa272", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "71335-2813", "generic_name": "hydroxychloroquine sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040150", "marketing_category": "ANDA", "marketing_start_date": "20250508", "listing_expiration_date": "20261231"}