NDC codes

FDA NDC Directory
Product NDC (as listed)31722-118Labeler and product segments. Claims need a package NDC.
Product NDC at billing width31722-0118Add 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
31722-118-313172201183125 VIAL, SINGLE-DOSE in 1 CARTON (31722-118-31) / 2 mL in 1 VIAL, SINGLE-DOSE (31722-118-02)Marketed from Nov 8, 2021
31722-118-323172201183225 VIAL, SINGLE-DOSE in 1 CARTON (31722-118-32) / 5 mL in 1 VIAL, SINGLE-DOSE (31722-118-05)Marketed from Nov 8, 2021
31722-118-333172201183310 VIAL, SINGLE-DOSE in 1 CARTON (31722-118-33) / 2 mL in 1 VIAL, SINGLE-DOSE (31722-118-02)Marketed from Apr 9, 2024
31722-118-343172201183410 VIAL, SINGLE-DOSE in 1 CARTON (31722-118-34) / 5 mL in 1 VIAL, SINGLE-DOSE (31722-118-05)Marketed from Apr 9, 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)
Lidocaine Hydrochloride
Generic name (nonproprietary)
lidocaine hydrochloride
Active ingredients
Lidocaine hydrochloride anhydrous — 20 mg/mL
Dosage form
Injection, Solution
Route
Epidural, Infiltration, Intracaudal, Perineural
Labeler
Camber Pharmaceuticals, Inc.NDC labeler code 31722
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214339
Marketing start
Listing expires
Other FDA classes
Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers
Product ID 31722-118_50208e47-95d1-c01a-e063-6294a90a7ecdSPL ID 50208e47-95d1-c01a-e063-6294a90a7ecdSPL set ID 7f202319-effa-4dd8-b871-e720b75f4a83RxCUI 1737562, 1737566, 1737568, 1737757, 1737761UNII EC2CNF7XFPUPC 0331722117029, 0331722118057, 0331722117050, 0331722117302, 0331722118026
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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N431722011831 followed by a unit qualifier and the quantity

Package 31722-0118-31. 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)

Lidocaine hydrochloride injection is indicated in adult and pediatric patients for the production of local or regional anesthesia or analgesia for surgery, dental, and oral surgery procedures, diagnostic and therapeutic procedures, and for obstetrical procedures. Specific concentrations and presentations of lidocaine hydrochloride injection are recommended for each type of block indicated to produce local or regional anesthesia or analgesia [see Dosage and Administration ( 2.2 )]. Lidocaine hydrochloride injection contains lidocaine, an amide local anesthetic. Lidocaine hydrochloride injection is indicated in adult and pediatric patients for the production of local or regional anesthesia or …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 31722-118

What is NDC 31722-118?
31722-118 is the product NDC for Lidocaine Hydrochloride, Lidocaine hydrochloride anhydrous 20 mg/mL injection, solution, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lidocaine Hydrochloride.
What is the active ingredient?
Lidocaine hydrochloride anhydrous.
Who is the labeler?
Camber Pharmaceuticals, Inc., NDC labeler code 31722. 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 Hydrochloride?
179 other product NDCs are listed under this name. See all Lidocaine Hydrochloride 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 Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Lidocaine HydrochlorideLidocaine hydrochloride 20 mg/mLSolutionOralMajor Pharmaceuticals0904-764400904-7644-87
Lidocaine HydrochlorideLidocaine 5 g/100gCreamTopicalYYBA CORP73581-12073581-0120-0173581-0120-0273581-0120-06
Lidocaine HydrochlorideLidocaine hydrochloride anhydrous 10 mg/mLInjection, SolutionInfiltration, PerineuralHenry Schein, Inc.0404-976300404-9763-20
lidocaine hydrochlorideLidocaine hydrochloride 10 mg/mLInjection, SolutionEpidural, Infiltration, Intracaudal, PerineuralAvenacy, LLC83634-65383634-0653-0283634-0653-0583634-0653-30
Lidocaine HydrochlorideLidocaine hydrochloride 10 mg/mLSolutionIntravenousBrookfield Pharmaceuticals, LLC.71351-02671351-0026-25
Lidocaine HydrochlorideLidocaine hydrochloride 20 mg/mLSolutionIntravenousBrookfield Pharmaceuticals, LLC.71351-02771351-0027-25
Lidocaine HydrochlorideLidocaine hydrochloride 10 mg/mLInjection, SolutionEpidural, Infiltration, Intracaudal, PerineuralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-94023155-0940-41
Lidocaine hydrochlorideLidocaine hydrochloride 20 mg/mLSolutionOral, TopicalAmerican Health Packaging60687-87060687-0870-64
Lidocaine HydrochlorideLidocaine hydrochloride 20 mg/mLSolutionOral, TopicalAurobindo Pharma Limited59651-94359651-0943-01
lidocaine hydrochlorideLidocaine hydrochloride 10 mg/mLInjection, SolutionInfiltration, PerineuralMedical Purchasing Solutions, LLC71872-736271872-7362-01

All 180 Lidocaine Hydrochloride NDCs

Other NDCs under ANDA 214339

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

FDA NDC Directory listings under ANDA 214339
ProductStrengthForm · routeLabelerProduct NDC
Lidocaine HydrochlorideLidocaine hydrochloride anhydrous 10 mg/mLInjection, SolutionEpidural, Infiltration, Intracaudal, PerineuralCamber Pharmaceuticals, Inc.31722-117

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