Endopan Hp Liquid
NDC Package 44911-0728-1
Package Information
Endopan Hp (aceticum acidum, alpha-lipoicum acidum, bryonia (alba), chromium, colchicum autumnale, lacticum acidum, lycopodium clavatum, phosphoricum acidum, phosphorus, sulphur, syzygium jambolanum, thuja occidentalis, uranium nitricum) liquids is adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0728.
Identification & Billing
Clinical Specifications
- ACETIC ACID 30 [hp_X]/mL
- ALPHA LIPOIC ACID 30 [hp_X]/mL
- BRYONIA ALBA ROOT 30 [hp_X]/mL
- CHROMIUM 30 [hp_X]/mL
- COLCHICUM AUTUMNALE BULB 30 [hp_X]/mL
- LACTIC ACID, DL- 30 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
- PHOSPHORIC ACID 30 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL
- SULFUR 30 [hp_X]/mL
- SYZYGIUM CUMINI SEED 30 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_X]/mL
- URANYL NITRATE HEXAHYDRATE 30 [hp_C]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0728 - Endopan Hp
- 44911-0728-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0728 - Endopan Hp
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 44911-0728-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Endopan Hp, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains acetic acid; alpha lipoic acid; bryonia alba root; chromium; colchicum autumnale bulb; lactic acid, dl-; lycopodium clavatum spore; phosphoric acid; phosphorus; sulfur; syzygium cumini seed; thuja occidentalis leafy twig; uranyl nitrate hexahydrate 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 January 24, 2025. 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: 44911072801. 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.