plaquenil
Generic: hydroxychloroquine sulfate
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
plaquenil
Generic Name
hydroxychloroquine sulfate
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
hydroxychloroquine sulfate 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-448
Product ID
71205-448_8aec894d-5711-4079-b167-240713bf04f2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA009768
Listing Expiration
2026-12-31
Marketing Start
2013-06-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205448
Hyphenated Format
71205-448
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
plaquenil (source: ndc)
Generic Name
hydroxychloroquine sulfate (source: ndc)
Application Number
NDA009768 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 12 TABLET in 1 BOTTLE (71205-448-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8aec894d-5711-4079-b167-240713bf04f2", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092", "979094"], "spl_set_id": ["8aec894d-5711-4079-b167-240713bf04f2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (71205-448-12)", "package_ndc": "71205-448-12", "marketing_start_date": "20200408"}], "brand_name": "Plaquenil", "product_id": "71205-448_8aec894d-5711-4079-b167-240713bf04f2", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "71205-448", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Plaquenil", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "NDA009768", "marketing_category": "NDA", "marketing_start_date": "20130628", "listing_expiration_date": "20261231"}