hydroxychloroquine sulfate
Generic: hydroxychloroquine sulfate
Labeler: cardinal health 107, llcDrug Facts
Product Profile
Brand Name
hydroxychloroquine sulfate
Generic Name
hydroxychloroquine sulfate
Labeler
cardinal health 107, llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
hydroxychloroquine sulfate 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55154-3567
Product ID
55154-3567_048ffc36-3b2f-4ce2-97dc-9dcb748b8d45
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210441
Listing Expiration
2026-12-31
Marketing Start
2018-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
551543567
Hyphenated Format
55154-3567
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
ANDA210441 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 10 BLISTER PACK in 1 BAG (55154-3567-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "048ffc36-3b2f-4ce2-97dc-9dcb748b8d45", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["e5fe2ece-40a1-49eb-818f-62ff3c3bb199"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-3567-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-3567-0", "marketing_start_date": "20180501"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "55154-3567_048ffc36-3b2f-4ce2-97dc-9dcb748b8d45", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "55154-3567", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA210441", "marketing_category": "ANDA", "marketing_start_date": "20180501", "listing_expiration_date": "20261231"}