NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0594Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0594Add 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
80425-0594-180425059401804250594011 TUBE in 1 CARTON (80425-0594-1) / 35.44 g in 1 TUBEMarketed from Sep 10, 2026

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)
Lidocaine
Generic name (nonproprietary)
lidocaine
Active ingredients
Lidocaine — 50 mg/g
Dosage form
Ointment
Route
Topical
Labeler
Advanced Rx of Tennessee, LLCNDC labeler code 80425
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 086724
Marketing start
Listing expires
Other FDA classes
Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers
Product ID 80425-0594_5b3b7337-37a1-b81e-e063-6394a90ac314SPL ID 5b3b7337-37a1-b81e-e063-6394a90ac314
Pharmacologic class
Amide Local Anesthetic; Antiarrhythmic

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

NDC on a medical claim

N480425059401 followed by a unit qualifier and the quantity

Package 80425-0594-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 80425-0594

What is NDC 80425-0594?
80425-0594 is the product NDC for Lidocaine, Lidocaine 50 mg/g ointment, listed with the FDA by Advanced Rx of Tennessee, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lidocaine.
What is the active ingredient?
Lidocaine.
Who is the labeler?
Advanced Rx of Tennessee, LLC, NDC labeler code 80425. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lidocaine?
160 other product NDCs are listed under this name. See all Lidocaine 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 Lidocaine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LidocaineLidocaine 50 mg/gOintmentTopicalDirect_Rx72189-69272189-0692-50
LidocaineLidocaine 50 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-419568788-4195-05
LidocaineLidocaine 50 mg/gPatchTopicalAscend Laboratories, LLC67877-76767877-0767-30
LidocaineLidocaine 80 mg/mLSprayTopicalYYBA CORP73581-90073581-0900-01
Lidocainelidocaine hydrochlorideLidocaine hydrochloride 20 mg/mLJellyTopicalSentiss Pharmaceuticals LLC70244-03970244-0039-0170244-0039-02
LidocaineLidocaine 100 kg/100kgGranuleTopicalShaanxi Shuvita Biotech Co., Ltd87879-00287879-0002-02
LidocainelidicaineLidocaine 50 mg/gOintmentTopicalEncube Ethicals, Inc.21922-10721922-0107-1321922-0107-61
LidocaineLidocaine hydrochloride 50 mg/mLGelTopicalYYBA Corp73581-11573581-0115-03
LidocaineLidocaine 5 g/100mLCreamTopicalYYBA Corp73581-02273581-0022-06
Lidocainelidocaine, mentholMenthol .1 g/10g; Lidocaine .4 g/10gPatchTransdermalVive Health LLC84722-307284722-3072-00

All 161 Lidocaine NDCs

Other NDCs under ANDA 086724

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 086724
ProductStrengthForm · routeLabelerProduct NDC
LidocaineLidocaine 50 mg/gOintmentTopicalATLANTIC BIOLOGICALS CORP.17856-3008
LidocaineLidocaine 50 mg/gOintmentTopicalDIRECT RX72189-165
LidocaineLidocaine 50 mg/gOintmentTopicalAdvanced Rx of Tennessee, LLC80425-0538
LidocaineLidocaine 50 mg/gOintmentTopicalPHOENIX RX LLC85509-3008
LidocaineLidocaine 50 mg/gOintmentTopicalGolden State Medical Supply, Inc.51407-383
LidocaineLidocaine 50 mg/gOintmentTopicalDIRECT RX72189-211
LidocaineLidocaine 50 mg/gOintmentTopicalNuCare Pharmaceuticals, Inc.68071-3792
LidocaineLidocaine 50 mg/gOintmentTopicalProficient Rx LP71205-288
LidocaineLidocaine 50 mg/gOintmentTopicalA-S Medication Solutions50090-8011
LidocaineLidocaine 50 mg/gOintmentTopicalQuality Care Products, LLC83008-044
LidocaineLidocaine 50 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-4050
LidocaineLidocaine 50 mg/gOintmentTopicalSun Pharmaceutical Industries, Inc.51672-3020
LidocaineLidocaine 50 mg/gOintmentTopicalSun Pharmaceutical Industries, Inc.51672-3008

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