What is NDC 44911-0070?

44911-0070 is the product NDC for Hepastat, Beta vulgaris whole 3 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Hepastat (Beta Vulgaris, Carduus Marianus, Taraxacum Officinale, Cholesterinum, Fel Tauri, Chelidonium Majus, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vomica, Phosphorus).

What is the active ingredient?

Beta vulgaris whole, Silybum marianum seed, Taraxacum officinale, Cholesterol, Bos taurus bile, Chelidonium majus whole, Lycopodium clavatum spore, Sodium sulfate, Strychnos nux-vomica seed, Phosphorus.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hepastat?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Hepastat NDC 44911-0070 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0070Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0070Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
44911-0070-1	4491100700144911007001	30 mL in 1 BOTTLE, DROPPER (44911-0070-1)Marketed from Apr 11, 2013

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Hepastat
Generic name (nonproprietary): beta vulgaris, carduus marianus, taraxacum officinale, cholesterinum, fel tauri, chelidonium majus, lycopodium clavatum, natrum sulphuricum, nux vomica, phosphorus
Active ingredients: Beta vulgaris whole — 3 [hp_X]/mLSilybum marianum seed — 3 [hp_X]/mLTaraxacum officinale — 3 [hp_X]/mLCholesterol — 6 [hp_X]/mLBos taurus bile — 6 [hp_X]/mLChelidonium majus whole — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLSodium sulfate — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 11, 2013
Marketing end: Sep 19, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 44911-0070_c9b9fe1c-76c6-4d0b-849b-55b6b0946507SPL ID c9b9fe1c-76c6-4d0b-849b-55b6b0946507SPL set ID d75ab44f-49cb-4a90-9e92-42457c603319UNII 4G174V5051, U946SH95EE, 39981FM375, 97C5T2UQ7J, ET3651ZLOU, 7E889U5RNN, C88X29Y479, 0YPR65R21J, 269XH13919, 27YLU75U4WUPC 0363113701098
Pharmacologic class: Non-Standardized Plant Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444911007001 followed by a unit qualifier and the quantity

Package 44911-0070-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective May 19, 2025.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve indigestion, flatulence, exhaustion, nausea and constipation.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 44911-0070

What is NDC 44911-0070?: 44911-0070 is the product NDC for Hepastat, Beta vulgaris whole 3 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hepastat (Beta Vulgaris, Carduus Marianus, Taraxacum Officinale, Cholesterinum, Fel Tauri, Chelidonium Majus, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vomica, Phosphorus).
What is the active ingredient?: Beta vulgaris whole, Silybum marianum seed, Taraxacum officinale, Cholesterol, Bos taurus bile, Chelidonium majus whole, Lycopodium clavatum spore, Sodium sulfate, Strychnos nux-vomica seed, Phosphorus.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hepastat?: 1 other product NDC are listed under this name. See all Hepastat NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Hepastat NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Hepastatbeta vulgaris, carduus marianus, taraxacum officinale, cholesterinum, cholinum, fel tauri, calcarea carbonica, chelidonium majus, lycopodium clavatum, mercurius solubilis, natrum sulphuricum, nux vomica, phosphorus	Beta vulgaris whole 3 [hp_X]/mL + 12 more ingredients	LiquidOral	Energique, Inc.	44911-0739	44911-0739-01