QIDILA 5% Minoxidil foam (minoxidil biiotin) NDC 85212-0036

Product information

Brand name (proprietary)

QIDILA 5% Minoxidil foam

Generic name (nonproprietary)

minoxidil biiotin

Active ingredients

Biotin — 5 g/100mLMinoxidil — 5 g/100mL

Dosage form

Aerosol, Foam

Route

Extracorporeal

Labeler

Beijing JUNGE Technology Co., Ltd.

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 075357

Marketing start

Jan 1, 2025

Listing expires

Dec 31, 2026

Other FDA classes

Arteriolar Vasodilation (Physiologic effect)

Identifiers

Product ID 85212-0036_3501c917-291e-9d4b-e063-6294a90a029cSPL ID 3501c917-291e-9d4b-e063-6294a90a029cSPL set ID 3501c917-291d-9d4b-e063-6294a90a029cRxCUI 2704021UNII 6SO6U10H04, 5965120SH1

Pharmacologic class

Arteriolar Vasodilator

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N485212003601 followed by a unit qualifier and the quantity Copy

Package 85212-0036-01. 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 075357

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