What is NDC 0781-8113?

0781-8113 is the product NDC for Bumetanide, Bumetanide 1 mg/1 tablet, listed with the FDA by Sandoz Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.

Sandoz Inc, NDC labeler code 0781. 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 0781-8113 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0781-8113Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00781-8113Add 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
0781-8113-01	0078181130100781811301	100 TABLET in 1 BOTTLE (0781-8113-01)Marketed from Jun 3, 2026
0781-8113-05	0078181130500781811305	500 TABLET in 1 BOTTLE (0781-8113-05)Marketed from Jun 3, 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: Sandoz IncNDC labeler code 0781
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074700
Marketing start: Jun 3, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers: Product ID 0781-8113_8914d8bf-61b7-4cd2-a8ef-7e1c5df37828SPL ID 8914d8bf-61b7-4cd2-a8ef-7e1c5df37828SPL set ID 8914d8bf-61b7-4cd2-a8ef-7e1c5df37828RxCUI 197417, 197418, 197419UNII 0Y2S3XUQ5HUPC 0307818113015, 0307818099012
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

N400781811301 followed by a unit qualifier and the quantity

Package 00781-8113-01. 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 Nov 16, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Bumetanide tablets, USP 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, USP 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 0781-8113

What is NDC 0781-8113?: 0781-8113 is the product NDC for Bumetanide, Bumetanide 1 mg/1 tablet, listed with the FDA by Sandoz Inc. 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?: Sandoz Inc, NDC labeler code 0781. 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 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
Bumetanide	Bumetanide .25 mg/mL	Injection, SolutionIntramuscular, Intravenous	Anthea Pharma Private Limited	83854-035	83854-0035-10

All 123 Bumetanide NDCs

Other NDCs under ANDA 074700

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

FDA NDC Directory listings under ANDA 074700
Product	Strength	Form · route	Labeler	Product NDC
Bumetanide	Bumetanide 1 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	43353-288
Bumetanide	Bumetanide 1 mg/1	TabletOral	Proficient Rx LP	82804-119
Bumetanide	Bumetanide 2 mg/1	TabletOral	Sandoz Inc	0781-8160
Bumetanide	Bumetanide 1 mg/1	TabletOral	Bryant Ranch Prepack	63629-4968
Bumetanide	Bumetanide .5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2195
Bumetanide	Bumetanide 1 mg/1	TabletOral	Bryant Ranch Prepack	72162-2196
Bumetanide	Bumetanide 2 mg/1	TabletOral	Bryant Ranch Prepack	72162-2197
Bumetanide	Bumetanide 1 mg/1	TabletOral	Bryant Ranch Prepack	71335-2670
Bumetanide	Bumetanide .5 mg/1	TabletOral	Sandoz Inc	0781-8099
Bumetanide	Bumetanide 1 mg/1	TabletOral	Bryant Ranch Prepack	71335-2920
Bumetanide	Bumetanide 2 mg/1	TabletOral	Bryant Ranch Prepack	71335-2705
Bumetanide	Bumetanide .5 mg/1	TabletOral	Sandoz Inc	0185-0128
Bumetanide	Bumetanide .5 mg/1	TabletOral	A-S Medication Solutions	50090-6308
Bumetanide	Bumetanide 2 mg/1	TabletOral	A-S Medication Solutions	50090-6304
Bumetanide	Bumetanide 1 mg/1	TabletOral	Sandoz Inc	0185-0129
Bumetanide	Bumetanide 2 mg/1	TabletOral	Sandoz Inc	0185-0130
Bumetanide	Bumetanide 2 mg/1	TabletOral	REMEDYREPACK INC.	70518-4387
Bumetanide	Bumetanide 1 mg/1	TabletOral	A-S Medication Solutions	50090-6345
Bumetanide	Bumetanide 2 mg/1	TabletOral	Bryant Ranch Prepack	71335-2998