Prescription drug · ANDA
bumetanide NDC 23155-900
Bumetanide .5 mg/1 · Tablet · Oral · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 23155-900-01 | 2315509000123155090001 | 100 TABLET in 1 BOTTLE (23155-900-01)Marketed from Jul 15, 2025 | |
| 23155-900-05 | 2315509000523155090005 | 500 TABLET in 1 BOTTLE (23155-900-05)Marketed from Jul 15, 2025 | |
| 23155-900-10 | 2315509001023155090010 | 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.NDC labeler code 23155
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 074225
- Marketing start
- Listing expires
- 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
N423155090001followed by a unit qualifier and the quantityPackage 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 . 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.
About NDC 23155-900
- What is NDC 23155-900?
- 23155-900 is the product NDC for bumetanide, Bumetanide .5 mg/1 tablet, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 3 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?
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. 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.
Related NDCs: other bumetanide products
Other finished products listed under the same name: strengths, forms and labelers.
| 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 |
Other NDCs under ANDA 074225
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| bumetanide | Bumetanide 1 mg/1 | TabletOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-901 |
| bumetanide | Bumetanide 2 mg/1 | TabletOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-902 |
| 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 |