Package 62135-752-90

Brand: hydroxychloroquine

Generic: hydroxychloroquine
NDC Package

Package Facts

Identity

Package NDC 62135-752-90
Digits Only 6213575290
Product NDC 62135-752
Product ID 62135-752_459cd828-6e8f-c7cf-e063-6394a90a5ab8
Description

90 TABLET in 1 BOTTLE (62135-752-90)

Marketing

Marketing Status
Marketed Since 2024-05-28
Brand hydroxychloroquine
Generic hydroxychloroquine
Sample Package No

Linked Drug Pages (1)

Hydroxychloroquine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459cd828-6e8f-c7cf-e063-6394a90a5ab8", "openfda": {"upc": ["0362135752903"], "unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["7e09aeca-0cec-4a88-9dde-a2098a08b877"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-752-90)", "package_ndc": "62135-752-90", "marketing_start_date": "20240528"}], "brand_name": "Hydroxychloroquine", "product_id": "62135-752_459cd828-6e8f-c7cf-e063-6394a90a5ab8", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "62135-752", "generic_name": "Hydroxychloroquine", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA210543", "marketing_category": "ANDA", "marketing_start_date": "20180706", "listing_expiration_date": "20261231"}