NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4478Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4478Add 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
70518-4478-07051844780090 TABLET in 1 BOTTLE, PLASTIC (70518-4478-0)Marketed from Sep 12, 2025

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)
Bumetanide
Generic name (nonproprietary)
bumetanide
Active ingredients
Bumetanide — 2 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213942
Marketing start
Listing expires
Other FDA classes
Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers
Product ID 70518-4478_5b39d53d-90f1-1a86-e063-6294a90ad1d9SPL ID 5b39d53d-90f1-1a86-e063-6294a90ad1d9
Pharmacologic class
Loop Diuretic

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470518447800 followed by a unit qualifier and the quantity

Package 70518-4478-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 213942

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

FDA NDC Directory listings under ANDA 213942
ProductStrengthForm · routeLabelerProduct NDC
BumetanideBumetanide .5 mg/1TabletOralNorthStar Rx LLC72603-889
BumetanideBumetanide 2 mg/1TabletOralNorthStar Rx LLC72603-901
BumetanideBumetanide 1 mg/1TabletOralNorthStar Rx LLC72603-900
BumetanideBumetanide .5 mg/1TabletOralAdvagen Pharma Limited72888-019
BumetanideBumetanide 1 mg/1TabletOralAdvagen Pharma Limited72888-020
BumetanideBumetanide 2 mg/1TabletOralAdvagen Pharma Limited72888-021
BumetanideBumetanide .5 mg/1TabletOralA-S Medication Solutions50090-7736
BumetanideBumetanide .5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8614
BumetanideBumetanide 1 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8615
BumetanideBumetanide 1 mg/1TabletOralREMEDYREPACK INC.70518-4385
BumetanideBumetanide 2 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8616

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Bumetanide NDC 70518-4478 | Med-Code