NDC codes

FDA NDC Directory
Product NDC (as listed)50090-2422Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-2422Add 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
50090-2422-0500902422002 VIAL, SINGLE-DOSE in 1 PACKAGE (50090-2422-0) / .1 mL in 1 VIAL, SINGLE-DOSEMarketed from Jan 24, 2017

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)
Narcan
Generic name (nonproprietary)
naloxone hydrochloride
Active ingredients
Naloxone hydrochloride — 4 mg/.1mL
Dosage form
Spray
Route
Nasal
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 208411
Marketing start
Listing expires
Other FDA classes
Opioid Antagonists (Mechanism)
Identifiers
Product ID 50090-2422_caf3eabb-89bd-469a-9d00-3fd3a18fb5dbSPL ID caf3eabb-89bd-469a-9d00-3fd3a18fb5dbSPL set ID 139c30b9-5600-48f5-8610-0cacd2782398RxCUI 1725059, 1725064UNII F850569PQR
Pharmacologic class
Opioid 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 HCPCS code in Med-Code's directory. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450090242200 followed by a unit qualifier and the quantity

Package 50090-2422-00. 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)

NARCAN Nasal Spray is indicated for the emergency treatment of known or suspected opioid overdose, as manifested by respiratory and/or central nervous system depression. NARCAN Nasal Spray is intended for immediate administration as emergency therapy in settings where opioids may be present. NARCAN Nasal Spray is not a substitute for emergency medical care. NARCAN Nasal Spray is an opioid antagonist indicated for the emergency treatment of known or suspected opioid overdose, as manifested by respiratory and/or central nervous system depression. ( 1 ) NARCAN Nasal Spray is intended for immediate administration as emergency therapy in settings where opioids may be present. ( 1 ) NARCAN Nasal S…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 208411

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

FDA NDC Directory listings under NDA 208411
ProductStrengthForm · routeLabelerProduct NDC
Narcannaloxone hydrochlorideNaloxone hydrochloride 4 mg/.1mLSprayNasalEmergent Devices Inc.69547-353
Narcannaloxone hydrochloride nasalNaloxone hydrochloride 4 mg/.1mLSprayNasalEmergent Devices Inc.69547-627
Naloxone Hydrochloridenaloxone hydrochloride nasalNaloxone hydrochloride 4 mg/.1mLInhalantNasalA-S Medication Solutions50090-5908
Narcan Naloxone HciNaloxone hydrochloride 4 mg/.1mLSprayNasalHF Acquisition Co LLC, DBA HealthFirst51662-1240
Narcannaloxone hydrochloride nasalNaloxone hydrochloride 4 mg/.1mLSprayNasalSportpharm LLC85766-076
Narcan Naloxone HCLNaloxone hydrochloride 4 mg/.1mLSprayNasalHF Acquisition Co LLC, DBA HealthFirst51662-1642
Narcannaloxone hydrochlorideNaloxone hydrochloride 4 mg/.1mLSprayNasalProficient Rx LP71205-528

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