Bumex (bumetanide) NDC 30698-630

NDC codes

FDA NDC Directory

Product NDC (as listed)30698-630Labeler and product segments. Claims need a package NDC.

Product NDC at billing width30698-0630Add 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
30698-630-01	30698063001	100 TABLET in 1 BOTTLE (30698-630-01)Marketed from Feb 28, 1983

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): Bumex
Generic name (nonproprietary): bumetanide
Active ingredients: Bumetanide — .5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Validus Pharmaceuticals LLC
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 018225
Marketing start: Feb 28, 1983
Listing expires: Dec 31, 2026
Other FDA classes: Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers: Product ID 30698-630_3e4799b2-7621-c0b4-e063-6394a90a47b7SPL ID 3e4799b2-7621-c0b4-e063-6394a90a47b7SPL set ID 32dfbea3-eb2b-4070-8605-57ce3e6d5a2fRxCUI 197417, 197418, 197419, 205488, 205489, 205490UNII 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

N430698063001 followed by a unit qualifier and the quantity

Package 30698-0630-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under NDA 018225

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

FDA NDC Directory listings under NDA 018225
Product	Strength	Form · route	Labeler	Product NDC
Bumetanide	Bumetanide 2 mg/1	TabletOral	American Health Packaging	60687-535
Bumetanide	Bumetanide .5 mg/1	TabletOral	Edenbridge Pharmaceuticals LLC.	42799-119
Bumetanide	Bumetanide 1 mg/1	TabletOral	Edenbridge Pharmaceuticals LLC.	42799-120
Bumetanide	Bumetanide 2 mg/1	TabletOral	Edenbridge Pharmaceuticals LLC.	42799-121
Bumexbumetanide	Bumetanide 1 mg/1	TabletOral	Validus Pharmaceuticals LLC	30698-631
Bumexbumetanide	Bumetanide 2 mg/1	TabletOral	Validus Pharmaceuticals LLC	30698-632
Bumetanide	Bumetanide 1 mg/1	TabletOral	American Health Packaging	60687-384