NDC codes

FDA NDC Directory
Product NDC (as listed)71872-7206Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71872-7206Add 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
71872-7206-1718727206011 VIAL, MULTI-DOSE in 1 BAG (71872-7206-1) / 10 mL in 1 VIAL, MULTI-DOSEMarketed from Feb 17, 2020

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)
Flumazenil
Generic name (nonproprietary)
flumazenil
Active ingredients
Flumazenil — .1 mg/mL
Dosage form
Injection
Route
Intravenous
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076755
Marketing start
Listing expires
Identifiers
Product ID 71872-7206_fad2ccdf-7cda-b25e-e053-6394a90addadSPL ID fad2ccdf-7cda-b25e-e053-6394a90addadSPL set ID 9f68c61a-c207-cdbe-e053-2a95a90af5a0RxCUI 204508UNII 40P7XK9392
Pharmacologic class
Benzodiazepine Antagonist

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.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N471872720601 followed by a unit qualifier and the quantity

Package 71872-7206-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Adult Patients: Flumazenil injection is indicated for the complete or partial reversal of the sedative effects of benzodiazepines in cases where general anesthesia has been induced and/or maintained with benzodiazepines, where sedation has been produced with benzodiazepines for diagnostic and therapeutic procedures, and for the management of benzodiazepine overdose. Pediatric Patients (aged 1 to 17): Flumazenil injection is indicated for the reversal of conscious sedation induced with benzodiazepines (see PRECAUTIONS: Pediatric Use ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076755

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

FDA NDC Directory listings under ANDA 076755
ProductStrengthForm · routeLabelerProduct NDC
FlumazenilFlumazenil .1 mg/mLInjectionIntravenousBaxter Healthcare Corporation36000-148
FlumazenilFlumazenil .1 mg/mLInjectionIntravenousBaxter Healthcare Corporation36000-149
FlumazenilFlumazenil .1 mg/mLInjectionIntravenousMedical Purchasing Solutions, LLC71872-7321

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