hydroxychloroquine sulfate
Generic: hydroxychloroquine sulfate
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
hydroxychloroquine sulfate
Generic Name
hydroxychloroquine sulfate
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
hydroxychloroquine sulfate 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-4465
Product ID
63629-4465_55eb56c0-c585-4373-a3a4-9276aaeae6d6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210441
Listing Expiration
2026-12-31
Marketing Start
2022-10-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636294465
Hyphenated Format
63629-4465
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
- 300 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (63629-4465-1)
- 14 TABLET in 1 BOTTLE (63629-4465-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "55eb56c0-c585-4373-a3a4-9276aaeae6d6", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["2569283"], "spl_set_id": ["2c109188-d28b-4c65-8b52-819bd8547f2e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-4465-1)", "package_ndc": "63629-4465-1", "marketing_start_date": "20240816"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (63629-4465-2)", "package_ndc": "63629-4465-2", "marketing_start_date": "20240816"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "63629-4465_55eb56c0-c585-4373-a3a4-9276aaeae6d6", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "63629-4465", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "300 mg/1"}], "application_number": "ANDA210441", "marketing_category": "ANDA", "marketing_start_date": "20221024", "listing_expiration_date": "20261231"}