What is NDC 0615-8615?

0615-8615 is the product NDC for Bumetanide, Bumetanide 1 mg/1 tablet, listed with the FDA by NCS HealthCare of KY, LLC dba Vangard Labs. It has 2 package NDCs, shown above in 10- and 11-digit form.

NCS HealthCare of KY, LLC dba Vangard Labs, NDC labeler code 0615. 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 0615-8615 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0615-8615Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00615-8615Add 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
0615-8615-05	0061586150500615861505	15 TABLET in 1 BLISTER PACK (0615-8615-05)Marketed from Jan 15, 2026
0615-8615-39	0061586153900615861539	30 TABLET in 1 BLISTER PACK (0615-8615-39)Marketed from Jan 15, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 1 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NCS HealthCare of KY, LLC dba Vangard LabsNDC labeler code 0615
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213942
Marketing start: Jan 16, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers: Product ID 0615-8615_dba39aec-7927-4310-a6d4-ee8de8b7163fSPL ID dba39aec-7927-4310-a6d4-ee8de8b7163fSPL set ID fa4e5faf-c91a-457b-bd2b-14a9add51ac8RxCUI 197417, 197418, 197419UNII 0Y2S3XUQ5H
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

N400615861505 followed by a unit qualifier and the quantity

Package 00615-8615-05. 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 Jan 21, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Bumetanide tablets are indicated for the treatment of edema associated with congestive heart failure, hepatic and renal disease, including the nephrotic syndrome. Almost equal diuretic response occurs after oral and parenteral administration of bumetanide. Therefore, if impaired gastrointestinal absorption is suspected or oral administration is not practical, bumetanide should be given by the intramuscular or intravenous route. Successful treatment with bumetanide tablets following instances of allergic reactions to furosemide suggests a lack of cross-sensitivity.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0615-8615

What is NDC 0615-8615?: 0615-8615 is the product NDC for Bumetanide, Bumetanide 1 mg/1 tablet, listed with the FDA by NCS HealthCare of KY, LLC dba Vangard Labs. It has 2 package NDCs, 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?: NCS HealthCare of KY, LLC dba Vangard Labs, NDC labeler code 0615. 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 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 2 mg/1	TabletOral	REMEDYREPACK INC.	70518-4478
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