NDC codes

FDA NDC Directory
Product NDC (as listed)53225-1111Labeler and product segments. Claims need a package NDC.
Product NDC at billing width53225-1111Add 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
53225-1111-3532251111035322511110328 POUCH in 1 CARTON (53225-1111-3) / 1 PATCH in 1 POUCH (53225-1111-1) / 1 SYSTEM in 1 PATCHMarketed from Sep 8, 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)
Bondlido
Generic name (nonproprietary)
lidocaine
Active ingredients
Lidocaine — 200 mg/1
Dosage form
System
Route
Topical
Labeler
Terrain Pharmaceuticals, Inc.NDC labeler code 53225
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 215029
Marketing start
Listing expires
Other FDA classes
Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers
Product ID 53225-1111_5cca5e32-619b-bb4a-e063-6294a90ad7bbSPL ID 5cca5e32-619b-bb4a-e063-6294a90ad7bb
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

N453225111103 followed by a unit qualifier and the quantity

Package 53225-1111-03. 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 53225-1111

What is NDC 53225-1111?
53225-1111 is the product NDC for Bondlido (lidocaine), Lidocaine 200 mg/1 system, listed with the FDA by Terrain Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Bondlido (Lidocaine).
What is the active ingredient?
Lidocaine.
Who is the labeler?
Terrain Pharmaceuticals, Inc., NDC labeler code 53225. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bondlido?
1 other product NDC are listed under this name. See all Bondlido 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 Bondlido NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
BondlidolidocaineLidocaine 200 mg/1SystemTopicalMEDRx USA, Inc.83708-11183708-0111-01

Other NDCs under NDA 215029

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

FDA NDC Directory listings under NDA 215029
ProductStrengthForm · routeLabelerProduct NDC
BondlidolidocaineLidocaine 200 mg/1SystemTopicalMEDRx USA, Inc.83708-111

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