Hydroxychloroquine sulfate NDC 65841-633

Product information

Brand name (proprietary)

Hydroxychloroquine sulfate

Generic name (nonproprietary)

hydroxychloroquine sulfate

Active ingredients

Hydroxychloroquine sulfate — 200 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Zydus Lifesciences Limited

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 040657

Marketing start

Jan 3, 2008

Listing expires

Dec 31, 2026

Identifiers

Product ID 65841-633_63d19fd8-9254-4f19-96a7-ec9fd9b0edd1SPL ID 63d19fd8-9254-4f19-96a7-ec9fd9b0edd1SPL set ID 1aa44bff-9a62-48b4-a520-98d7d524e3a9RxCUI 979092UNII 8Q2869CNVH

Pharmacologic class

Antimalarial; Antirheumatic Agent

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N465841063301 followed by a unit qualifier and the quantity Copy

Package 65841-0633-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Other NDCs under ANDA 040657

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.