hydroxychloroquine sulfate
Generic: hydroxychloroquine sulfate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
hydroxychloroquine sulfate
Generic Name
hydroxychloroquine sulfate
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
hydroxychloroquine sulfate 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6280
Product ID
50090-6280_e3ddf397-4b8f-40cf-adbc-d1f056fc27a6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213342
Listing Expiration
2026-12-31
Marketing Start
2020-05-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906280
Hyphenated Format
50090-6280
Supplemental Identifiers
RxCUI
UNII
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
ANDA213342 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (50090-6280-1)
- 90 TABLET in 1 BOTTLE (50090-6280-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3ddf397-4b8f-40cf-adbc-d1f056fc27a6", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["b4dca05a-745f-4c15-b731-1e99176cf44c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6280-1)", "package_ndc": "50090-6280-1", "marketing_start_date": "20221215"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6280-2)", "package_ndc": "50090-6280-2", "marketing_start_date": "20221215"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "50090-6280_e3ddf397-4b8f-40cf-adbc-d1f056fc27a6", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "50090-6280", "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": "ANDA213342", "marketing_category": "ANDA", "marketing_start_date": "20200512", "listing_expiration_date": "20261231"}