bumetanide NDC 23155-900

NDC codes

FDA NDC Directory

Product NDC (as listed)23155-900Labeler and product segments. Claims need a package NDC.

Product NDC at billing width23155-0900Add 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
23155-900-01	23155090001	100 TABLET in 1 BOTTLE (23155-900-01)Marketed from Jul 15, 2025
23155-900-05	23155090005	500 TABLET in 1 BOTTLE (23155-900-05)Marketed from Jul 15, 2025
23155-900-10	23155090010	1000 TABLET in 1 BOTTLE (23155-900-10)Marketed from Jul 15, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — .5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074225
Marketing start: Jul 15, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers: Product ID 23155-900_ee0c44ac-10ca-4d9b-98f0-1342fc97dd39SPL ID ee0c44ac-10ca-4d9b-98f0-1342fc97dd39SPL set ID d4688d53-9baf-4cf0-b37f-47779bce7815RxCUI 197417, 197418, 197419UNII 0Y2S3XUQ5HUPC 0323155901016, 0323155902013, 0323155900019
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

N423155090001 followed by a unit qualifier and the quantity

Package 23155-0900-01. 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 Jul 11, 2025. 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)

Other NDCs under ANDA 074225

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

FDA NDC Directory listings under ANDA 074225
Product	Strength	Form · route	Labeler	Product NDC
bumetanide	Bumetanide .5 mg/1	TabletOral	NorthStar Rx, LLC	72603-297
bumetanide	Bumetanide 1 mg/1	TabletOral	NorthStar Rx, LLC	72603-298
bumetanide	Bumetanide 2 mg/1	TabletOral	NorthStar Rx, LLC	72603-299
bumetanide	Bumetanide 2 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-902
bumetanide	Bumetanide 1 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-901