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  5. NDC Package Code: 85212-0036-1 Qidila 5% Minoxidil Foam

NDC Package 85212-0036-1 Qidila 5% Minoxidil Foam

Minoxidil Biiotin Aerosol, Foam Extracorporeal - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
85212-0036-1
Package Description:
60 mL in 1 BOTTLE, PUMP
Product Code:
85212-0036
Proprietary Name:
Qidila 5% Minoxidil Foam
Non-Proprietary Name:
Minoxidil Biiotin
Substance Name:
Biotin; Minoxidil
Usage Information:
Use to regrow hair on the top of the scalp
11-Digit NDC Billing Format:
85212003601
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Beijing Junge Technology Co., Ltd.
Dosage Form:
Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
Administration Route(s):
Extracorporeal - Administration outside of the body.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA075357
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
01-01-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 85212-0036-1?

The NDC Packaged Code 85212-0036-1 is assigned to a package of 60 ml in 1 bottle, pump of Qidila 5% Minoxidil Foam, a human over the counter drug labeled by Beijing Junge Technology Co., Ltd.. The product's dosage form is aerosol, foam and is administered via extracorporeal form.

Is NDC 85212-0036 included in the NDC Directory?

Yes, Qidila 5% Minoxidil Foam with product code 85212-0036 is active and included in the NDC Directory. The product was first marketed by Beijing Junge Technology Co., Ltd. on January 01, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85212-0036-1?

The 11-digit format is 85212003601. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-185212-0036-15-4-285212-0036-01