What is NDC 59088-905?

59088-905 is the product NDC for Lidocan (lidocaine 5%), Lidocaine 700 mg/1 patch, listed with the FDA by PURETEK CORPORATION. It has 2 package NDCs, shown above in 10- and 11-digit form.

PURETEK CORPORATION, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Lidocan?

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.

Lidocan NDC 59088-905 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-905Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0905Add 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 NDC	11-digit (billing)	Package	Copy
59088-905-54	5908809055459088090554	30 POUCH in 1 PACKAGE (59088-905-54) / 1 PATCH in 1 POUCH (59088-905-84)Marketed from Jul 14, 2023
59088-905-82	5908809058259088090582	15 POUCH in 1 PACKAGE (59088-905-82) / 1 PATCH in 1 POUCH (59088-905-84)Marketed from Jan 27, 2026

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): Lidocan
Generic name (nonproprietary): lidocaine 5%
Active ingredients: Lidocaine — 700 mg/1
Dosage form: Patch
Route: Topical
Labeler: PURETEK CORPORATIONNDC labeler code 59088
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209190
Marketing start: May 14, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers: Product ID 59088-905_48891c0c-2eb2-a114-e063-6294a90a61bbSPL ID 48891c0c-2eb2-a114-e063-6294a90a61bbSPL set ID fd8e4856-3785-4850-e053-6294a90a95b6RxCUI 1745091, 2642344UNII 98PI200987UPC 0359088905821
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

N459088090554 followed by a unit qualifier and the quantity

Package 59088-0905-54. 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 Jan 27, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE LIDOCAN™ 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 59088-905

What is NDC 59088-905?: 59088-905 is the product NDC for Lidocan (lidocaine 5%), Lidocaine 700 mg/1 patch, listed with the FDA by PURETEK CORPORATION. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Lidocan (Lidocaine 5%).
What is the active ingredient?: Lidocaine.
Who is the labeler?: PURETEK CORPORATION, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lidocan?: 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.

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
Product	Strength	Form · route	Labeler	Product NDC
Lidocaine 5%	Lidocaine 50 mg/g	PatchTopical	Asclemed USA, Inc.	76420-899
Lidocaine 5%	Lidocaine 50 mg/g	PatchTopical	St. Mary's Medical Park Pharmacy	60760-657
Lidocaine 5%	Lidocaine 700 mg/1	PatchTopical	NuCare Pharmaceuticals,Inc.	68071-3620
Lidocaine 5%	Lidocaine 50 mg/g	PatchTopical	REMEDYREPACK INC.	70518-4487
Lidocan Vlidocaine 5%	Lidocaine 50 mg/g	PatchTopical	PURETEK CORPORATION	59088-909
Lidocan VIIlidocaine 5%	Lidocaine 50 mg/g	PatchTopical	PURETEK CORPORATION	59088-900
Lidocan IIIlidocaine 5%	Lidocaine 50 mg/g	PatchTopical	PURETEK CORPORATION	59088-907
Lidocan IVlidocaine 5%	Lidocaine 50 mg/g	PatchTopical	PURETEK CORPORATION	59088-910
Lidocan VIlidocaine 5%	Lidocaine 50 mg/g	PatchTopical	PURETEK CORPORATION	59088-911
Lidocaine 5% Patchlidocaine 5%	Lidocaine 700 mg/1	PatchTopical	Medcore LLC	82461-611
Lidocaine 5%	Lidocaine 50 mg/g	PatchTopical	YARAL Pharma Inc.	82347-0505
Lidox 5 Patchlidocaine 5% patch	Lidocaine 50 mg/g	PatchTopical	Injecta Medcial LLC	87234-0505
Lidocaine 5%	Lidocaine 50 mg/g	PatchTopical	A-S Medication Solutions	50090-7857
Tridacaine XLlidocaine	Lidocaine 50 mg/g	PatchTopical	Trifluent Pharma LLC	73352-845
Tridacaine IIIlidocaine	Lidocaine 50 mg/g	PatchTopical	Trifluent Pharma LLC	73352-835

Lidocan (Lidocaine 5%) NDC 59088-905