N09 Bacterotox NDC 63479-1409

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-1409Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-1409Add 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
63479-1409-1	63479140901	30 mL in 1 BOTTLE, GLASS (63479-1409-1)Marketed from Dec 15, 1994

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): N09 BacterotoxSuffix: BACTEROTOX
Generic name (nonproprietary): aconitum napellus, allium cepa, allium sativum, belladonna, calcarea sulphurica, calendula officinalis, echinacea angustifolia, ferrum phosphoricum, calcium sulfide, hydrastis canadensis, lachesis mutus, myristica sebifera, silicea, thuja occidentalis
Active ingredients: Silicon dioxide — 12 [hp_X]/mLOnion — 30 [hp_X]/mLCalendula officinalis flowering top — 1 [hp_X]/mLEchinacea angustifolia — 1 [hp_X]/mLCalcium sulfide — 200 [hp_X]/mLLachesis muta venom — 90 [hp_X]/mLFerrosoferric phosphate — 60 [hp_X]/mLGoldenseal — 1 [hp_X]/mLAconitum napellus — 200 [hp_X]/mLGarlic — 30 [hp_X]/mLAtropa belladonna — 200 [hp_X]/mLVirola sebifera resin — 2 [hp_X]/mLThuja occidentalis leafy twig — 90 [hp_X]/mLCalcium sulfate anhydrous — 60 [hp_X]/mL
Dosage form: Solution/ drops
Route: Sublingual
Labeler: Apex Energetics Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 15, 1994
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Phosphate Chelating Activity (Mechanism)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 63479-1409_0e773c6a-0172-fae5-e063-6294a90af595SPL ID 0e773c6a-0172-fae5-e063-6294a90af595SPL set ID ba99bb1e-c36f-8bf8-e053-2995a90ac308UNII ETJ7Z6XBU4, 492225Q21H, 18E7415PXQ, VB06AV5US8, 1MBW07J51Q, VSW71SS07I, 91GQH8I5F7, ZW3Z11D0JV, U0NQ8555JD, V1V998DC17, WQZ3G9PF0H, GHJ5XX5SGS, 1NT28V9397, E934B3V59HUPC 0818960013035
Pharmacologic class: Blood Coagulation Factor; Non-Standardized Food Allergenic Extract; Phosphate Binder

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463479140901 followed by a unit qualifier and the quantity

Package 63479-1409-01. 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

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