Hepastat Liquid
NDC Package 44911-0739-1
Package Information
Hepastat (beta vulgaris, carduus marianus, taraxacum officinale, cholesterinum, cholinum, fel tauri, calcarea carbonica, chelidonium majus, lycopodium clavatum, mercurius solubilis, natrum sulphuricum, nux vomica, phosphorus) 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 44911-0739.
Identification & Billing
Clinical Specifications
- BETA VULGARIS WHOLE 3 [hp_X]/mL
- BOS TAURUS BILE 6 [hp_X]/mL
- CHELIDONIUM MAJUS WHOLE 12 [hp_X]/mL
- CHOLESTEROL 6 [hp_X]/mL
- CHOLINE HYDROXIDE 6 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- MERCURIUS SOLUBILIS 12 [hp_X]/mL
- MILK THISTLE 3 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL
- SODIUM SULFATE 12 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
- TARAXACUM OFFICINALE 3 [hp_X]/mL
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0739 - Hepastat
- 44911-0739-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0739 - Hepastat
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 44911-0739-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Hepastat, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains beta vulgaris whole; bos taurus bile; chelidonium majus whole; cholesterol; choline hydroxide; lycopodium clavatum spore; mercurius solubilis; milk thistle; oyster shell calcium carbonate, crude; phosphorus; sodium sulfate; strychnos nux-vomica seed; taraxacum officinale 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 March 06, 2026. The current certification is valid through December 31, 2027.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911073901. 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.