Endopar Liquid
NDC Package 44911-0440-1
Package Information
Endopar (glandula suprarenalis suis, hypophysis suis, hypothalamus suis, oophorinum (suis), orchitinum (bovine), pineal gland, thyroidinum, arsenicum album, baryta carbonica, natrum muriaticum, phosphoricum acidum, pulsatilla (pratensis)) liquids May temporarily relieve nervous exhaustion, mental sluggishness, weak pulse, cold hands and feet, muscular exhaustion, and may help those easily fatigued.****Claims based on traditional homeopathic practice, not accepted medical evidence. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0440.
Identification & Billing
Clinical Specifications
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- BARIUM CARBONATE 12 [hp_X]/mL
- BOS TAURUS TESTICLE 8 [hp_X]/mL
- PHOSPHORIC ACID 12 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 12 [hp_X]/mL
- SODIUM CHLORIDE 12 [hp_X]/mL
- SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
- SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
- SUS SCROFA OVARY 8 [hp_X]/mL
- SUS SCROFA PINEAL GLAND 8 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND 8 [hp_X]/mL
- THYROID 8 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0440 - Endopar
- 44911-0440-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0440 - Endopar
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 the distribution configuration for this product package?
The code 44911-0440-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Endopar, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arsenic trioxide; barium carbonate; bos taurus testicle; phosphoric acid; pulsatilla pratensis whole; sodium chloride; sus scrofa adrenal gland; sus scrofa hypothalamus; sus scrofa ovary; sus scrofa pineal gland; sus scrofa pituitary gland; thyroid 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 Energique, Inc. on July 19, 2018. The current certification is valid through December 31, 2026.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911044001. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.