NDC codes

FDA NDC Directory
Product NDC (as listed)76420-524Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76420-0524Add 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
76420-524-0176420052401764200524011 KIT in 1 CARTON (76420-524-01) * 25 VIAL in 1 CARTON (70121-1049-5) / 1 mL in 1 VIAL * .33 mL in 1 AMPULE * 100 PACKET in 1 BOX (53329-941-30) / 1 mL in 1 PACKET * 10 AMPULE in 1 CARTON (55150-158-72) / 2 mL in 1 AMPULEMarketed from Jul 1, 2013

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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

Generic name (nonproprietary)
ammonia, lidocaine hydrochloride, triamcinolone acetonide, povidone-iodine
Dosage form
Kit
Labeler
Asclemed USA, Inc.NDC labeler code 76420
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 76420-524_23b3dfe1-6de6-e847-e063-6294a90a3e7eSPL ID 23b3dfe1-6de6-e847-e063-6294a90a3e7eSPL set ID e25cfc22-29ba-473f-88c4-3c88e9f6863bRxCUI 797730, 1299889, 1737568, 1792144

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N476420052401 followed by a unit qualifier and the quantity

Package 76420-0524-01. 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 AND USAGE Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including triamcinolone acetonide injectable suspension is indicated for intramuscular use as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders: Primary …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 76420-524

What is NDC 76420-524?
76420-524 is the product NDC for Physician EZ Use Joint Tunnel and Trigger Kit kit, listed with the FDA by Asclemed USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Physician EZ Use Joint Tunnel and Trigger Kit (Ammonia, Lidocaine hydrochloride, Triamcinolone acetonide, Povidone-iodine).
Who is the labeler?
Asclemed USA, Inc., NDC labeler code 76420. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Physician EZ Use Joint Tunnel and Trigger Kit?
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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