NDC codes

FDA NDC Directory
Product NDC (as listed)43742-1787Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43742-1787Add 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
43742-1787-14374217870130 mL in 1 BOTTLE, DROPPER (43742-1787-1)Marketed from May 14, 2021

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)
Lym Combination
Generic name (nonproprietary)
anaplasma phagocytophilum, babesia microti, bartonella henselae, borrelia burgdorferi nosode, ehrlichia nosode (canine), mycoplasma pneumoniae, morbillinum, meningococcus nosode, hepatitis b nosode
Active ingredients
Anaplasma phagocytophilum — 15 [hp_X]/mLBabesia microti — 15 [hp_X]/mLBartonella henselae — 15 [hp_X]/mLBorrelia burgdorferi — 15 [hp_X]/mLEhrlichia canis — 15 [hp_X]/mLMycoplasma pneumoniae — 15 [hp_X]/mLMeasles virus — 16 [hp_X]/mLNeisseria meningitidis — 27 [hp_X]/mLHepatitis b virus — 15 [hp_C]/mL
Dosage form
Liquid
Route
Oral
Labeler
Deseret Biologicals, Inc.NDC labeler code 43742
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 43742-1787_582e4d54-3964-415d-beaf-bed5b109c868SPL ID 582e4d54-3964-415d-beaf-bed5b109c868SPL set ID 2a0b6ec2-ead1-4260-8447-4a2d04275d0cUNII BHE5668847, 1948X6KEG3, 84PG7W9845, 0J8NV9V5Q8, 970Y8T1JZY, JQE470FAD0, HT3R7C012Q, V3TP2MD7F3, 77H9EM77P7UPC 0810151882277

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

N443742178701 followed by a unit qualifier and the quantity

Package 43742-1787-01. 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)

USES: • For the temporarily relief of symptoms including: • joint pain • headaches • fever • flu symptoms • difficulty chewing • muscle aches • stiff neck • change in smell and taste These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43742-1787

What is NDC 43742-1787?
43742-1787 is the product NDC for Lym Combination, Anaplasma phagocytophilum 15 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lym Combination (Anaplasma Phagocytophilum, Babesia Microti, Bartonella Henselae, Borrelia Burgdorferi Nosode, Ehrlichia Nosode (Canine), Mycoplasma Pneumoniae, Morbillinum, Meningococcus Nosode, Hepatitis B Nosode).
What is the active ingredient?
Anaplasma phagocytophilum, Babesia microti, Bartonella henselae, Borrelia burgdorferi, Ehrlichia canis, Mycoplasma pneumoniae, Measles virus, Neisseria meningitidis, Hepatitis b virus.
Who is the labeler?
Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lym Combination?
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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Lym Combination NDC 43742-1787 | National Drug Code | Med-Code