NDC codes

FDA NDC Directory
Product NDC (as listed)44911-0488Labeler and product segments. Claims need a package NDC.
Product NDC at billing width44911-0488Add 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 NDC11-digit (billing)PackageCopy
44911-0488-1449110488014491104880130 mL in 1 BOTTLE, DROPPER (44911-0488-1)Marketed from Feb 22, 2019

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)
Thyrostat
Generic name (nonproprietary)
fucus vesiculosus, spongia tosta, hypophysis suis, thyroidinum (suis), arsenicum iodatum, baryta carbonica, iodium, lycopus virginicus, natrum muriaticum
Active ingredients
Fucus vesiculosus — 3 [hp_X]/mLSpongia officinalis skeleton, Roasted — 3 [hp_X]/mLSus scrofa pituitary gland — 6 [hp_X]/mLThyroid — 6 [hp_X]/mLArsenic triiodide — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLIodine — 12 [hp_X]/mLLycopus virginicus — 12 [hp_X]/mLSodium chloride — 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
Listing expires
Identifiers
Product ID 44911-0488_fddfa4f5-e354-49fc-ac87-1e2d94a592f2SPL ID fddfa4f5-e354-49fc-ac87-1e2d94a592f2SPL set ID 5c41b36c-e28f-4d60-b9b9-6b888d55ea95UNII 535G2ABX9M, 1PIP394IID, L0PFEMQ1DT, 6RV024OAUQ, 3029988O2T, 6P669D8HQ8, 2E32821G6I, 9679TC07X4, TWH5125Q6F, 451W47IQ8XUPC 0363113701401

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

N444911048801 followed by a unit qualifier and the quantity

Package 44911-0488-01. 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 .

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve difficulty swallowing, flushed face, glaring eyes, excited mental state or nervousness.** **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 44911-0488

What is NDC 44911-0488?
44911-0488 is the product NDC for Thyrostat, Fucus vesiculosus 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?
Thyrostat (Fucus Vesiculosus, Spongia Tosta, Hypophysis Suis, Thyroidinum (Suis), Arsenicum Iodatum, Baryta Carbonica, Iodium, Lycopus Virginicus, Natrum Muriaticum).
What is the active ingredient?
Fucus vesiculosus, Spongia officinalis skeleton, Roasted, Sus scrofa pituitary gland, Thyroid, Arsenic triiodide, Barium carbonate, Oyster shell calcium carbonate, Crude, Iodine, Lycopus virginicus, Sodium chloride.
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 Thyrostat?
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.

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