hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydroxychloroquine sulfate
Generic Name hydroxychloroquine sulfate
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

hydroxychloroquine sulfate 200 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7306
Product ID 50090-7306_b75f9502-33e8-4f7f-9e12-4ca4e673e794
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040657
Listing Expiration 2026-12-31
Marketing Start 2008-01-03

Pharmacologic Class

Classes
antimalarial [epc] antirheumatic agent [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907306
Hyphenated Format 50090-7306

Supplemental Identifiers

RxCUI
979092
UNII
8Q2869CNVH

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name hydroxychloroquine sulfate (source: ndc)
Generic Name hydroxychloroquine sulfate (source: ndc)
Application Number ANDA040657 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-7306-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7306-2)
source: ndc

Packages (2)

50090-7306-1 60 TABLET, FILM COATED in 1 BOTTLE (50090-7306-1) 50090-7306-2 90 TABLET, FILM COATED in 1 BOTTLE (50090-7306-2)

Ingredients (1)

hydroxychloroquine sulfate (200 mg/1)

Linked Drug Pages (1)

Hydroxychloroquine sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b75f9502-33e8-4f7f-9e12-4ca4e673e794", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["3817387f-2fc8-4f39-8096-3b48fff57ab0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7306-1)", "package_ndc": "50090-7306-1", "marketing_start_date": "20241014"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7306-2)", "package_ndc": "50090-7306-2", "marketing_start_date": "20241014"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "50090-7306_b75f9502-33e8-4f7f-9e12-4ca4e673e794", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "50090-7306", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "A-S Medication Solutions", "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": "20080103", "listing_expiration_date": "20261231"}