NDC codes

FDA NDC Directory
Product NDC (as listed)73352-845Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73352-0845Add 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
73352-845-307335208453030 PACKET in 1 BOX (73352-845-30) / 1 g in 1 PACKET (73352-845-01)Marketed from Sep 20, 2024

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

Brand name (proprietary)
Tridacaine XL
Generic name (nonproprietary)
lidocaine
Active ingredients
Lidocaine50 mg/g
Dosage form
Patch
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209190
Marketing start
Listing expires
Other FDA classes
Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers
Product ID 73352-845_a94ac408-bd85-4a3e-90fb-123c3788a25fSPL ID a94ac408-bd85-4a3e-90fb-123c3788a25fSPL set ID 032b37a7-8a47-4809-a330-c76314225cbdRxCUI 1745091, 2678310UNII 98PI200987UPC 0373352845309
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

N473352084530 followed by a unit qualifier and the quantity

Package 73352-0845-30. 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)

INDICATION AND USAGE Lidocaine patch 5% is indicated for relief of pain associated with post-herpetic neuralgia. It should be applied only to intact skin.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209190

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

FDA NDC Directory listings under ANDA 209190
ProductStrengthForm · routeLabelerProduct NDC
Lidocaine 5%Lidocaine 50 mg/gPatchTopicalSt. Mary's Medical Park Pharmacy60760-657
Lidocaine 5%Lidocaine 700 mg/1PatchTopicalNuCare Pharmaceuticals,Inc.68071-3620
Lidox 5 Patchlidocaine 5% patchLidocaine 50 mg/gPatchTopicalInjecta Medcial LLC87234-0505
Lidocaine 5%Lidocaine 50 mg/gPatchTopicalREMEDYREPACK INC.70518-4487
Lidocaine 5% Patchlidocaine 5%Lidocaine 700 mg/1PatchTopicalMedcore LLC82461-611
Lidocaine 5%Lidocaine 50 mg/gPatchTopicalYARAL Pharma Inc.82347-0505
Tridacaine IIIlidocaineLidocaine 50 mg/gPatchTopicalTrifluent Pharma LLC73352-835
Lidocanlidocaine 5%Lidocaine 700 mg/1PatchTopicalPURETEK CORPORATION59088-905
Lidocan VIIlidocaine 5%Lidocaine 50 mg/gPatchTopicalPURETEK CORPORATION59088-900
Lidocan VIlidocaine 5%Lidocaine 50 mg/gPatchTopicalPURETEK CORPORATION59088-911
Lidocan IIIlidocaine 5%Lidocaine 50 mg/gPatchTopicalPURETEK CORPORATION59088-907
Lidocan Vlidocaine 5%Lidocaine 50 mg/gPatchTopicalPURETEK CORPORATION59088-909
Lidocan IVlidocaine 5%Lidocaine 50 mg/gPatchTopicalPURETEK CORPORATION59088-910
Lidocaine 5%Lidocaine 50 mg/gPatchTopicalA-S Medication Solutions50090-7857
Lidocaine 5%Lidocaine 50 mg/gPatchTopicalAsclemed USA, Inc.76420-899

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