Gallbladderpar NDC 44911-0256

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0256Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0256Add 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
44911-0256-1	44911025601	30 mL in 1 BOTTLE, DROPPER (44911-0256-1)Marketed from Sep 3, 2015

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): Gallbladderpar
Generic name (nonproprietary): carduus marianus, fel tauri, taraxacum officinale, chelidonium majus, lycopodium clavatum, magnesia phosphorica, natrum sulphuricum, nux vomica, phosphorus, sanguinaria canadensis, gallbladder (suis)
Active ingredients: Milk thistle — 3 [hp_X]/mLBos taurus bile — 6 [hp_X]/mLTaraxacum officinale — 6 [hp_X]/mLChelidonium majus whole — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 12 [hp_X]/mLSodium sulfate — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLSanguinaria canadensis root — 12 [hp_X]/mLSus scrofa gallbladder — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 3, 2015
Marketing end: Dec 6, 2028
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 44911-0256_a61319f8-c3b0-44bd-a702-1e1796e378d1SPL ID a61319f8-c3b0-44bd-a702-1e1796e378d1SPL set ID 1d68d6b0-a018-4450-af3c-103b976b4617UNII U946SH95EE, ET3651ZLOU, 39981FM375, 7E889U5RNN, C88X29Y479, HF539G9L3Q, 0YPR65R21J, 269XH13919, 27YLU75U4W, N9288CD508, B6A98VOI9IUPC 0363113701500
Pharmacologic class: Calculi Dissolution Agent; Non-Standardized Plant Allergenic Extract; Osmotic Laxative

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

N444911025601 followed by a unit qualifier and the quantity

Package 44911-0256-01. 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 Jul 31, 2026.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms of flatulence, constipation, belching, abdominal discomfort, and burning and itching due to hemorrhoids.** **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)