Metabopath Liquid
NDC Package 64578-0102-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Metabopath (adenosinum cyclophosphoricum, adenosinum triphosphoricum dinatrum, alpha-ketoglutaricum acidum, berberis vulgaris, citricum acidum, coenzyme a, dna, fumaricum acidum, glycyrrhiza glabra, hepar sulphuris calcareum, lappa major, magnesia phosphorica, manganum aceticum, nadidum, natrum muriaticum, natrum oxalaceticum, natrum pyruvicum, nicotinamidum, pulsatilla, pyridoxinum hydrochloricum, rhamnus purshiana, riboflavinum, rna, silicea, succinicum acidum, sulphur, thiaminum hydrochloricum,) liquids is classified as a

administered via oral route. This formulation utilizes a liquid delivery system. Marketed by Energetix Corporation, this product is identified by NDC 64578-0102.

Identification & Billing

NDC Package Code
64578-0102-1
Package Description
59.1 mL in 1 BOTTLE, DROPPER
Product Code
64578-0102
11-Digit Billing Format
64578010201

Clinical Specifications

Proprietary Name
Metabopath
Non-Proprietary Name
Adenosinum Cyclophosphoricum, Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Berberis Vulgaris, Citricum Acidum, Coenzyme A, Dna, Fumaricum Acidum, Glycyrrhiza Glabra, Hepar Sulphuris Calcareum, Lappa Major, Magnesia Phosphorica, Manganum Aceticum, Nadidum, Natrum Muriaticum, Natrum Oxalaceticum, Natrum Pyruvicum, Nicotinamidum, Pulsatilla, Pyridoxinum Hydrochloricum, Rhamnus Purshiana, Riboflavinum, Rna, Silicea, Succinicum Acidum, Sulphur, Thiaminum Hydrochloricum,
Substance Name
Adenosine Cyclic Phosphate; .alpha.-ketoglutaric Acid; Adenosine Triphosphate Disodium; Berberis Vulgaris Root Bark; Anhydrous Citric Acid; Coenzyme A; Herring Sperm Dna; Fumaric Acid; Glycyrrhiza Glabra; Calcium Sulfide; Arctium Lappa Root; Magnesium Phosphate, Dibasic; Manganese Acetate Tetrahydrate; Nadide; Sodium Chloride; Sodium Diethyl Oxalacetate; Sodium Pyruvate; Niacinamide; Pulsatilla Vulgaris; Pyridoxine Hydrochloride; Frangula Purshiana Bark; Riboflavin; Saccharomyces Cerevisiae Rna; Silicon Dioxide; Succinic Acid; Sulfur; Thiamine Hydrochloride; Thyroid, Bovine; Trifolium Pratense Flower; Zanthoxylum Americanum Bark; Zinc Gluconate
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class

Regulatory & Marketing

Labeler Name
Energetix Corporation
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
08-08-2014
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 64578-0102-1 identifies a specific commercial package of 59.1 ml in 1 bottle, dropper of Metabopath, a human over the counter drug labeled by Energetix Corporation. This liquid is formulated for oral use and contains adenosine cyclic phosphate; .alpha.-ketoglutaric acid; adenosine triphosphate disodium; berberis vulgaris root bark; anhydrous citric acid; coenzyme a; herring sperm dna; fumaric acid; glycyrrhiza glabra; calcium sulfide; arctium lappa root; magnesium phosphate, dibasic; manganese acetate tetrahydrate; nadide; sodium chloride; sodium diethyl oxalacetate; sodium pyruvate; niacinamide; pulsatilla vulgaris; pyridoxine hydrochloride; frangula purshiana bark; riboflavin; saccharomyces cerevisiae rna; silicon dioxide; succinic acid; sulfur; thiamine hydrochloride; thyroid, bovine; trifolium pratense flower; zanthoxylum americanum bark; zinc gluconate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Energetix Corporation on August 08, 2014. The current certification is valid through December 31, 2027.

How is this Energetix Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 64578010201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
64578-0102-1
11-Digit CMS (5-4-2)
64578-0102-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.