NDC Package 44911-0675-1 Anxiety HP

Aconitum Napellus,Argentum Nitricum,Arsenicum Album,Calcarea Carbonica,Ignatia Amara,Kali - 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:
44911-0675-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Anxiety HP
Non-Proprietary Name:
Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Calcarea Carbonica, Ignatia Amara, Kali Carbonicum, Lachesis Mutus, Natrum Muriaticum, Phosphorus, Pulsatilla (pratensis), Staphysagria, Stramonium
Substance Name:
Aconitum Napellus Whole; Arsenic Trioxide; Datura Stramonium; Delphinium Staphisagria Seed; Lachesis Muta Venom; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Potassium Carbonate; Pulsatilla Pratensis Whole; Silver Nitrate; Sodium Chloride; Strychnos Ignatii Seed
Usage Information:
• Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. • Consult a physician for use in children under 12 years of age.Store in a cool, dry place.
11-Digit NDC Billing Format:
44911067501
Product Type:
Human Otc Drug
Labeler Name:
Energique, Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
06-09-2023
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 44911-0675-1?

The NDC Packaged Code 44911-0675-1 is assigned to a package of 30 ml in 1 bottle, dropper of Anxiety HP, a human over the counter drug labeled by Energique, Inc.. The product's dosage form is liquid and is administered via oral form.

Is NDC 44911-0675 included in the NDC Directory?

Yes, Anxiety HP with product code 44911-0675 is active and included in the NDC Directory. The product was first marketed by Energique, Inc. on June 09, 2023 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 44911-0675-1?

The 11-digit format is 44911067501. 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
5-4-144911-0675-15-4-244911-0675-01