1. Home
  2. Labeler Index
  3. Biologische Heilmittel Heel
  4. 51885-7030
  5. NDC Package Code: 51885-7030-1 .alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root

NDC Package 51885-7030-1 .alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root

Injection - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
51885-7030-1
Package Description:
1000 AMPULE in 1 BOX / 2 mL in 1 AMPULE
Product Code:
51885-7030
Non-Proprietary Name:
.alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root
Substance Name:
Alpha Lipoic Acid; Arnica Montana Root; Coenzyme A; Nadide; Sanguinaria Canadensis Root; Sodium Diethyl Oxalacetate; Solanum Dulcamara Top; Sulfur; Sus Scrofa Cartilage; Sus Scrofa Embryo; Sus Scrofa Placenta; Sus Scrofa Umbilical Cord; Toxicodendron Pubescens Leaf
11-Digit NDC Billing Format:
51885703001
Product Type:
Bulk Ingredient
Labeler Name:
Biologische Heilmittel Heel
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Active Ingredient(s):
  • ALPHA LIPOIC ACID 8 [hp_X]/2mL
  • ARNICA MONTANA ROOT 4 [hp_X]/2mL
  • COENZYME A 8 [hp_X]/2mL
  • NADIDE 8 [hp_X]/2mL
  • SANGUINARIA CANADENSIS ROOT 4 [hp_X]/2mL
  • SODIUM DIETHYL OXALACETATE 8 [hp_X]/2mL
  • SOLANUM DULCAMARA TOP 3 [hp_X]/2mL
  • SULFUR 6 [hp_X]/2mL
  • SUS SCROFA CARTILAGE 6 [hp_X]/2mL
  • SUS SCROFA EMBRYO 6 [hp_X]/2mL
  • SUS SCROFA PLACENTA 6 [hp_X]/2mL
  • SUS SCROFA UMBILICAL CORD 6 [hp_X]/2mL
  • TOXICODENDRON PUBESCENS LEAF 2 [hp_X]/2mL
    • Sample Package:
    N/A
    Marketing Category:
    DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
    Start Marketing Date:
    04-30-2018
    End Marketing Date:
    12-31-2024
    Exclude Flag:
    N
    Unfinished Product:
    Yes
    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 51885-7030-1?

    The NDC Packaged Code 51885-7030-1 is assigned to an UNFINISHED drug package of 1000 ampule in 1 box / 2 ml in 1 ampule of .alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root, a bulk ingredient labeled by Biologische Heilmittel Heel. The product's dosage form is injection and is administered via form.

    Is NDC 51885-7030 included in the NDC Directory?

    Yes, .alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root is an UNFINISHED PRODUCT with code 51885-7030 that is active and included in the NDC Directory. The product was first marketed by Biologische Heilmittel Heel on April 30, 2018.

    What is the 11-digit format for NDC 51885-7030-1?

    The 11-digit format is 51885703001. 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
    5-4-151885-7030-15-4-251885-7030-01