What is NDC 44911-0535?

44911-0535 is the product NDC for Thyropar, 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?

Thyropar (Fucus Vesiculosus, Spongia Tosta, Glandula Suprarenalis Suis, Hypophysis Suis, Thyroidinum (Suis), Bromium, Calcarea Carbonica, Iodium, Lachesis Mutus, Pulsatilla (Pratensis)).

What is the active ingredient?

Fucus vesiculosus, Spongia officinalis skeleton, Roasted, Sus scrofa adrenal gland, Sus scrofa pituitary gland, Sus scrofa thyroid, Bromine, Oyster shell calcium carbonate, Crude, Iodine, Lachesis muta venom, Anemone pratensis.

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 Thyropar?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Thyropar NDC 44911-0535 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0535Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0535Add 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
44911-0535-1	4491105350144911053501	30 mL in 1 BOTTLE, DROPPER (44911-0535-1)Marketed from Mar 2, 2020

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): Thyropar
Generic name (nonproprietary): fucus vesiculosus, spongia tosta, glandula suprarenalis suis, hypophysis suis, thyroidinum (suis), bromium, calcarea carbonica, iodium, lachesis mutus, pulsatilla (pratensis)
Active ingredients: Fucus vesiculosus — 3 [hp_X]/mLSpongia officinalis skeleton, Roasted — 3 [hp_X]/mLSus scrofa adrenal gland — 6 [hp_X]/mLSus scrofa pituitary gland — 6 [hp_X]/mLSus scrofa thyroid — 6 [hp_X]/mLBromine — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLIodine — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLAnemone pratensis — 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: Mar 2, 2020
Marketing end: Dec 7, 2026
Identifiers: Product ID 44911-0535_1387214b-6ef9-4562-aa90-3a7c31bd7c61SPL ID 1387214b-6ef9-4562-aa90-3a7c31bd7c61SPL set ID 9482ff15-15b2-4c1f-ae15-24f6d810254eUNII 535G2ABX9M, 1PIP394IID, 398IYQ16YV, L0PFEMQ1DT, 6RV024OAUQ, SBV4XY874G, 2E32821G6I, 9679TC07X4, VSW71SS07I, 8E272251DI

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

N444911053501 followed by a unit qualifier and the quantity

Package 44911-0535-01. 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 Oct 30, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve exhaustion and heaviness of the body, dry rough skin, dry cough, difficulty swallowing and swollen throat.** **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 44911-0535

What is NDC 44911-0535?: 44911-0535 is the product NDC for Thyropar, 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?: Thyropar (Fucus Vesiculosus, Spongia Tosta, Glandula Suprarenalis Suis, Hypophysis Suis, Thyroidinum (Suis), Bromium, Calcarea Carbonica, Iodium, Lachesis Mutus, Pulsatilla (Pratensis)).
What is the active ingredient?: Fucus vesiculosus, Spongia officinalis skeleton, Roasted, Sus scrofa adrenal gland, Sus scrofa pituitary gland, Sus scrofa thyroid, Bromine, Oyster shell calcium carbonate, Crude, Iodine, Lachesis muta venom, Anemone pratensis.
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 Thyropar?: 1 other product NDC are listed under this name. See all Thyropar 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 Thyropar NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Thyroparfucus vesiculosus, spongia tosta, glandula suprarenalis suis, hypophysis suis, thyroidinum (suis), bromium, calcarea carbonica, graphites, iodium, lachesis mutus, levothyroxinum, pulsatilla (pratensis), selenium metallicum	Fucus vesiculosus 3 [hp_X]/mL + 12 more ingredients	LiquidOral	Energique, Inc.	44911-0683	44911-0683-01