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  5. NDC Package Code: 68466-9490-4 Alpha Cf

NDC Package 68466-9490-4 Alpha Cf

Aconitum Napellus,Bryonia Alba Root,Eucalyptus Globulus Leaf,Eupatorium Perfoliatum - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
68466-9490-4
Package Description:
1 BLISTER PACK in 1 BOX / 40 TABLET in 1 BLISTER PACK
Product Code:
68466-9490
Proprietary Name:
Alpha Cf
Non-Proprietary Name:
Aconitum Napellus, Bryonia Alba Root, Eucalyptus Globulus Leaf, Eupatorium Perfoliatum Flowering Top, Gelsemium Sempervirens Root, Ipecac, Phosphorus
Substance Name:
Aconitum Napellus; Bryonia Alba Root; Eucalyptus Globulus Leaf; Eupatorium Perfoliatum Flowering Top; Gelsemium Sempervirens Root; Ipecac; Phosphorus
Usage Information:
Indication and Usage:Uses: Temporarily relieves these symptoms: fever, chills, sneezing, stuffed-up nose, runny nose, coughing, sore throat, headache, minor aches and pains.
11-Digit NDC Billing Format:
68466949004
Product Type:
Human Otc Drug
Labeler Name:
Schwabe Mexico, S.a. De C.v.
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Sublingual - Administration beneath the tongue.
Active Ingredient(s):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
07-13-2018
End Marketing Date:
09-30-2025
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
68466-9490-14 BLISTER PACK in 1 BOX / 10 TABLET in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68466-9490-4?

The NDC Packaged Code 68466-9490-4 is assigned to a package of 1 blister pack in 1 box / 40 tablet in 1 blister pack of Alpha Cf, a human over the counter drug labeled by Schwabe Mexico, S.a. De C.v.. The product's dosage form is tablet and is administered via sublingual form.

Is NDC 68466-9490 included in the NDC Directory?

Yes, Alpha Cf with product code 68466-9490 is active and included in the NDC Directory. The product was first marketed by Schwabe Mexico, S.a. De C.v. on July 13, 2018.

What is the 11-digit format for NDC 68466-9490-4?

The 11-digit format is 68466949004. 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
5-4-168466-9490-45-4-268466-9490-04