hydroxychloroquine

Generic: hydroxychloroquine

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydroxychloroquine
Generic Name hydroxychloroquine
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydroxychloroquine sulfate 200 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-752
Product ID 62135-752_459cd828-6e8f-c7cf-e063-6394a90a5ab8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210543
Listing Expiration 2026-12-31
Marketing Start 2018-07-06

Pharmacologic Class

Classes
antimalarial [epc] antirheumatic agent [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135752
Hyphenated Format 62135-752

Supplemental Identifiers

RxCUI
979092
UPC
0362135752903
UNII
8Q2869CNVH

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name hydroxychloroquine (source: ndc)
Application Number ANDA210543 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (62135-752-90)
source: ndc

Packages (1)

62135-752-90 90 TABLET in 1 BOTTLE (62135-752-90)

Ingredients (1)

hydroxychloroquine sulfate (200 mg/1)

Linked Drug Pages (1)

Hydroxychloroquine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459cd828-6e8f-c7cf-e063-6394a90a5ab8", "openfda": {"upc": ["0362135752903"], "unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["7e09aeca-0cec-4a88-9dde-a2098a08b877"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-752-90)", "package_ndc": "62135-752-90", "marketing_start_date": "20240528"}], "brand_name": "Hydroxychloroquine", "product_id": "62135-752_459cd828-6e8f-c7cf-e063-6394a90a5ab8", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "62135-752", "generic_name": "Hydroxychloroquine", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA210543", "marketing_category": "ANDA", "marketing_start_date": "20180706", "listing_expiration_date": "20261231"}