NDC Package 0363-2070-14 Miconazole 3

Miconazole Nitrate Cream Vaginal - View Billable Units, 11-Digit Format, RxNorm

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:
0363-2070-14
Package Description:
3 APPLICATOR in 1 CARTON / 5 g in 1 APPLICATOR
Product Code:
Proprietary Name:
Miconazole 3
Non-Proprietary Name:
Miconazole Nitrate
Substance Name:
Miconazole Nitrate
Usage Information:
This medication is used to treat vaginal yeast infections. Miconazole reduces vaginal burning, itching, and discharge that may occur with this condition. This medication is an azole antifungal. It works by stopping the growth of yeast (fungus) that causes the infection. The vaginal product comes in 2 forms (a vaginal cream or tablet). Some products also come with a skin cream to be applied to the area around the outside of the vagina. Ask your doctor before using this medication for self-treatment if this is your first vaginal infection. This medication only works for vaginal fungal infections. You may have a different type of infection (such as bacterial vaginosis) and may need a different medication. If you have fever, chills, flu-like symptoms, stomach/abdominal pain, or a bad-smelling vaginal discharge, do not use this medication. Contact your doctor right away because these may be signs of a more serious infection.
11-Digit NDC Billing Format:
00363207014
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Walgreen Company
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Vaginal - Administration into the vagina.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
ANDA091366
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-15-2018
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.

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Frequently Asked Questions

What is NDC 0363-2070-14?

The NDC Packaged Code 0363-2070-14 is assigned to a package of 3 applicator in 1 carton / 5 g in 1 applicator of Miconazole 3, a human over the counter drug labeled by Walgreen Company. The product's dosage form is cream and is administered via vaginal form.

Is NDC 0363-2070 included in the NDC Directory?

Yes, Miconazole 3 with product code 0363-2070 is active and included in the NDC Directory. The product was first marketed by Walgreen Company on June 15, 2018 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 0363-2070-14?

The 11-digit format is 00363207014. 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 4-4-2 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
4-4-20363-2070-145-4-200363-2070-14