NDC codes

FDA NDC Directory
Product NDC (as listed)71872-7095Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71872-7095Add 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
71872-7095-1718727095011 VIAL, MULTI-DOSE in 1 BAG (71872-7095-1) / 50 mL in 1 VIAL, MULTI-DOSEMarketed from Feb 26, 2019

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 Hydrochloride
Generic name (nonproprietary)
lidocaine hydrochloride
Active ingredients
Lidocaine hydrochloride — 20 mg/mL
Dosage form
Injection, Solution
Route
Infiltration, Perineural
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 088327
Marketing start
Listing expires
Other FDA classes
Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers
Product ID 71872-7095_fc5e932d-0841-7ad9-e053-6394a90af784SPL ID fc5e932d-0841-7ad9-e053-6394a90af784SPL set ID 858f3faa-e56e-51f9-e053-2a91aa0aa721RxCUI 1010671UNII V13007Z41A
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

N471872709501 followed by a unit qualifier and the quantity

Package 71872-7095-01. 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)

INDICATIONS AND USAGE Lidocaine Hydrochloride Injection, USP is indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks, when the accepted procedures for these techniques as described in standard textbooks are observed.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 088327

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

FDA NDC Directory listings under ANDA 088327
ProductStrengthForm · routeLabelerProduct NDC
2% Lidocaine HciLidocaine hydrochloride 20 mg/mLInjection, SolutionInfiltration, PerineuralHF Acquisition Co LLC, DBA HealthFirst51662-1467
Lidocaine HydrochlorideLidocaine hydrochloride 20 mg/mLInjection, SolutionInfiltration, PerineuralHospira, Inc.0409-4277
2% Lidocaine HciLidocaine hydrochloride 20 mg/mLInjection, SolutionInfiltration, PerineuralHF Acquisition Co LLC, DBA HealthFirst51662-1326
Lidocaine HydrochlorideLidocaine hydrochloride 20 mg/mLInjection, SolutionInfiltration, PerineuralProPharma Distribution84549-277
Lidocaine Hydrochloridelidocaine hydrochloride anhydrousLidocaine hydrochloride 20 mg/mLInjection, SolutionInfiltration, PerineuralHenry Schein, Inc.0404-9895
Lidocaine HydrochlorideLidocaine hydrochloride 20 mg/mLInjection, SolutionInfiltration, PerineuralMedical Purchasing Solutions, LLC71872-7125

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