What is NDC 44911-0449?

44911-0449 is the product NDC for Systemistat, Berberis vulgaris root bark 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?

Systemistat (Berberis Vulgaris, Chelidonium Majus, Lappa Major, Hydrastis Canadensis, Hepar Sulphuris Calcareum, Lycopodium Clavatum, Sulphur, Calcarea Carbonica, Mercurius Solubilis, Thuja Occidentalis).

What is the active ingredient?

Berberis vulgaris root bark, Chelidonium majus whole, Arctium lappa root, Goldenseal, Calcium sulfide, Lycopodium clavatum spore, Sulfur, Oyster shell calcium carbonate, Crude, Mercurius solubilis, Thuja occidentalis leafy twig.

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 Systemistat?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Systemistat NDC 44911-0449 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0449Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0449Add 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
44911-0449-1	4491104490144911044901	30 mL in 1 BOTTLE, DROPPER (44911-0449-1)Marketed from Mar 6, 2018

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): Systemistat
Generic name (nonproprietary): berberis vulgaris, chelidonium majus, lappa major, hydrastis canadensis, hepar sulphuris calcareum, lycopodium clavatum, sulphur, calcarea carbonica, mercurius solubilis, thuja occidentalis
Active ingredients: Berberis vulgaris root bark — 3 [hp_X]/mLChelidonium majus whole — 3 [hp_X]/mLArctium lappa root — 3 [hp_X]/mLGoldenseal — 5 [hp_X]/mLCalcium sulfide — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLMercurius solubilis — 30 [hp_X]/mLThuja occidentalis leafy twig — 30 [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: Mar 6, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0449_babfa6e6-4ea6-4937-af61-795cc3cb257eSPL ID babfa6e6-4ea6-4937-af61-795cc3cb257eSPL set ID 0d8aa575-3fae-4828-8827-d2561672a91eUNII 1TH8Q20J0U, 7E889U5RNN, 597E9BI3Z3, ZW3Z11D0JV, 1MBW07J51Q, C88X29Y479, 70FD1KFU70, 2E32821G6I, 324Y4038G2, 1NT28V9397UPC 0363113700657

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

N444911044901 followed by a unit qualifier and the quantity

Package 44911-0449-01. 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 Apr 21, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptons of fatigue, brain fog, sinus congestion, lymphatic congestion, poor digestion or eczema with itching.** **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 44911-0449

What is NDC 44911-0449?: 44911-0449 is the product NDC for Systemistat, Berberis vulgaris root bark 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?: Systemistat (Berberis Vulgaris, Chelidonium Majus, Lappa Major, Hydrastis Canadensis, Hepar Sulphuris Calcareum, Lycopodium Clavatum, Sulphur, Calcarea Carbonica, Mercurius Solubilis, Thuja Occidentalis).
What is the active ingredient?: Berberis vulgaris root bark, Chelidonium majus whole, Arctium lappa root, Goldenseal, Calcium sulfide, Lycopodium clavatum spore, Sulfur, Oyster shell calcium carbonate, Crude, Mercurius solubilis, Thuja occidentalis leafy twig.
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 Systemistat?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.