Package 16714-110-02

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 16714-110-02
Digits Only 1671411002
Product NDC 16714-110
Product ID 16714-110_09ec5070-4e0b-4cf5-b3f1-67c0152b84a5
Description

500 TABLET, FILM COATED in 1 BOTTLE (16714-110-02)

Marketing

Marketing Status
Marketed Since 2021-12-03
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": "09ec5070-4e0b-4cf5-b3f1-67c0152b84a5", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["29ba0172-7ca3-4122-af1b-f0da522318cb"], "manufacturer_name": ["Northstar Rx LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-110-01)", "package_ndc": "16714-110-01", "marketing_start_date": "20191001"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16714-110-02)", "package_ndc": "16714-110-02", "marketing_start_date": "20211203"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "16714-110_09ec5070-4e0b-4cf5-b3f1-67c0152b84a5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "16714-110", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "Northstar Rx LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040657", "marketing_category": "ANDA", "marketing_start_date": "20191001", "listing_expiration_date": "20261231"}