NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1971Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1971Add 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
71335-1971-1713351971017133519710130 PATCH in 1 POUCH (71335-1971-1)Marketed from Oct 21, 2021
71335-1971-271335197102713351971023 PATCH in 1 POUCH (71335-1971-2)Marketed from Oct 21, 2021
71335-1971-371335197103713351971039 PATCH in 1 POUCH (71335-1971-3)Marketed from Oct 21, 2021
71335-1971-4713351971047133519710410 PATCH in 1 POUCH (71335-1971-4)Marketed from Oct 21, 2021
71335-1971-5713351971057133519710514 PATCH in 1 POUCH (71335-1971-5)Marketed from Oct 21, 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)
Lidocaine
Generic name (nonproprietary)
lidocaine
Active ingredients
Lidocaine — 700 mg/1
Dosage form
Patch
Route
Topical
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206463
Marketing start
Listing expires
Other FDA classes
Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers
Product ID 71335-1971_03bcee4d-5c75-4224-bed0-7484506eeadaSPL ID 03bcee4d-5c75-4224-bed0-7484506eeadaSPL set ID b4db5684-988f-44c4-a81e-5c04b8b0f6e7RxCUI 1745091UNII 98PI200987
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

N471335197101 followed by a unit qualifier and the quantity

Package 71335-1971-01. 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)

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)

About NDC 71335-1971

What is NDC 71335-1971?
71335-1971 is the product NDC for Lidocaine, Lidocaine 700 mg/1 patch, listed with the FDA by Bryant Ranch Prepack. It has 5 package NDCs, 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?
Bryant Ranch Prepack, NDC labeler code 71335. 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 50 mg/gOintmentTopicalAdvanced Rx of Tennessee, LLC80425-059480425-0594-01
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

All 161 Lidocaine NDCs

Other NDCs under ANDA 206463

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

FDA NDC Directory listings under ANDA 206463
ProductStrengthForm · routeLabelerProduct NDC
LidocaineLidocaine 700 mg/1PatchTopicalPHOENIX RX LLC85509-1791
LidocaineLidocaine 700 mg/1PatchTopicalPreferred Pharmaceuticals Inc.68788-8344
LidocaineLidocaine 700 mg/1PatchTopicalAdvanced Rx Pharmacy of Tennessee, LLC80425-0325
LidocaineLidocaine 700 mg/1PatchTopicalA-S Medication Solutions50090-7894
LidocaineLidocaine 700 mg/1PatchTopicalSportpharm LLC85766-170
LidocaineLidocaine 700 mg/1PatchTopicalAvKARE42291-477
LidocaineLidocaine 700 mg/1PatchTopicalBryant Ranch Prepack72162-2085
LidocaineLidocaine 700 mg/1PatchTopicalASCLEMED USA INC.87063-273
Lidocaine PatchLidocaine 700 mg/1PatchTopicalDirect_Rx72189-387
LidocaineLidocaine 700 mg/1PatchTopicalAmneal Pharmaceuticals LLC65162-791

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