What is NDC 70518-4478?

70518-4478 is the product NDC for Bumetanide, Bumetanide 2 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bumetanide?

122 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Bumetanide NDC 70518-4478 | National Drug Code

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 NDC	11-digit (billing)	Package	Copy
70518-4478-0	7051844780070518447800	90 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
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213942
Marketing start: Sep 12, 2025
Listing expires: Dec 31, 2027
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.

About NDC 70518-4478

What is NDC 70518-4478?: 70518-4478 is the product NDC for Bumetanide, Bumetanide 2 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bumetanide.
What is the active ingredient?: Bumetanide.
Who is the labeler?: REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bumetanide?: 122 other product NDCs are listed under this name. See all Bumetanide 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 Bumetanide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Bumetanide	Bumetanide .5 mg/1	TabletOral	Sandoz Inc	0781-8099	00781-8099-0100781-8099-05
Bumetanide	Bumetanide 1 mg/1	TabletOral	Sandoz Inc	0781-8113	00781-8113-0100781-8113-05
Bumetanide	Bumetanide 2 mg/1	TabletOral	Sandoz Inc	0781-8160	00781-8160-01
Bumetanide	Bumetanide .25 mg/mL	Injection, SolutionIntramuscular, Intravenous	Civica, Inc.	72572-210	72572-0210-10
Bumetanide	Bumetanide .25 mg/mL	Injection, SolutionIntramuscular, Intravenous	Civica, Inc.	72572-211	72572-0211-10
Bumetanide	Bumetanide .25 mg/mL	InjectionIntramuscular, Intravenous	Cardinal Health 107, LLC	55154-5131	55154-5131-05
Bumetanide	Bumetanide 1 mg/1	TabletOral	NorthStar Rx LLC	72603-900	72603-0900-0172603-0900-02
Bumetanide	Bumetanide .5 mg/1	TabletOral	NorthStar Rx LLC	72603-889	72603-0889-01
Bumetanide	Bumetanide 2 mg/1	TabletOral	NorthStar Rx LLC	72603-901	72603-0901-0172603-0901-02
Bumetanide	Bumetanide .25 mg/mL	Injection, SolutionIntramuscular, Intravenous	Anthea Pharma Private Limited	83854-007	83854-0007-10

All 123 Bumetanide NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Bumetanide	Bumetanide .5 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8614
Bumetanide	Bumetanide 1 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8615
Bumetanide	Bumetanide 2 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8616
Bumetanide	Bumetanide .5 mg/1	TabletOral	A-S Medication Solutions	50090-7736
Bumetanide	Bumetanide 1 mg/1	TabletOral	REMEDYREPACK INC.	70518-4385
Bumetanide	Bumetanide .5 mg/1	TabletOral	NorthStar Rx LLC	72603-889
Bumetanide	Bumetanide 1 mg/1	TabletOral	NorthStar Rx LLC	72603-900
Bumetanide	Bumetanide 2 mg/1	TabletOral	NorthStar Rx LLC	72603-901
Bumetanide	Bumetanide .5 mg/1	TabletOral	Advagen Pharma Limited	72888-019
Bumetanide	Bumetanide 1 mg/1	TabletOral	Advagen Pharma Limited	72888-020
Bumetanide	Bumetanide 2 mg/1	TabletOral	Advagen Pharma Limited	72888-021