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 50090-4659
Product ID 50090-4659_755581f8-6167-46af-991f-9cb92a16d06c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210577
Listing Expiration 2027-12-31
Marketing Start 2018-05-17

Pharmacologic Class

Classes
antimalarial [epc] antirheumatic agent [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904659
Hyphenated Format 50090-4659

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 ANDA210577 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-4659-2)
  • 12 TABLET, FILM COATED in 1 BOTTLE (50090-4659-3)
source: ndc

Packages (2)

50090-4659-2 90 TABLET, FILM COATED in 1 BOTTLE (50090-4659-2) 50090-4659-3 12 TABLET, FILM COATED in 1 BOTTLE (50090-4659-3)

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": "755581f8-6167-46af-991f-9cb92a16d06c", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["87076a61-ce76-475b-ac6d-c33ba617195d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4659-2)", "package_ndc": "50090-4659-2", "marketing_start_date": "20191028"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (50090-4659-3)", "package_ndc": "50090-4659-3", "marketing_start_date": "20200317"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "50090-4659_755581f8-6167-46af-991f-9cb92a16d06c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "50090-4659", "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": "ANDA210577", "marketing_category": "ANDA", "marketing_start_date": "20180517", "listing_expiration_date": "20271231"}