What is NDC 17856-3294?

17856-3294 is the product NDC for Furosemide, Furosemide 10 mg/mL solution, listed with the FDA by Atlantic Biologicals Corp.. It has 1 package NDC, shown above in 10- and 11-digit form.

Atlantic Biologicals Corp., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Furosemide?

204 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Furosemide NDC 17856-3294 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17856-3294Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17856-3294Add 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
17856-3294-1	1785632940117856329401	120 SYRINGE in 1 CASE (17856-3294-1) / 3 mL in 1 SYRINGEMarketed from Jun 23, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Furosemide
Generic name (nonproprietary): furosemide
Active ingredients: Furosemide — 10 mg/mL
Dosage form: Solution
Route: Oral
Labeler: Atlantic Biologicals Corp.NDC labeler code 17856
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 070434
Marketing start: Jul 12, 1988
Listing expires: Dec 31, 2027
Other FDA classes: Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers: Product ID 17856-3294_54ed0de5-046f-06d7-e063-6394a90ad3b6SPL ID 54ed0de5-046f-06d7-e063-6394a90ad3b6SPL set ID 54ed0dd9-2fa8-269a-e063-6294a90a607cRxCUI 197730UNII 7LXU5N7ZO5
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

N417856329401 followed by a unit qualifier and the quantity

Package 17856-3294-01. 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 Jun 23, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Edema Furosemide is indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver and renal disease, including the nephrotic syndrome. Furosemide is particularly useful when an agent with greater diuretic potential is desired. Hypertension Oral furosemide may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. Hypertensive patients who cannot be adequately controlled with thiazides will probably also not be adequately controlled with furosemide alone.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17856-3294

What is NDC 17856-3294?: 17856-3294 is the product NDC for Furosemide, Furosemide 10 mg/mL solution, listed with the FDA by Atlantic Biologicals Corp.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Furosemide.
What is the active ingredient?: Furosemide.
Who is the labeler?: Atlantic Biologicals Corp., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Furosemide?: 204 other product NDCs are listed under this name. See all Furosemide 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 Furosemide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Furosemide	Furosemide 10 mg/mL	InjectionIntramuscular, Intravenous	Civica, Inc.	72572-275	72572-0275-10
Furosemide	Furosemide 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4679	70518-4679-00
Furosemide	Furosemide 20 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-033	87441-0033-01
Furosemide	Furosemide 20 mg/1	TabletOral	Coupler LLC	67046-0768	67046-0768-03
Furosemide	Furosemide 40 mg/1	TabletOral	REMEDYREPACK INC.	70518-4609	70518-4609-00
Furosemide	Furosemide 40 mg/1	TabletOral	Coupler LLC	67046-1663	67046-1663-03
Furosemide	Furosemide 20 mg/1	TabletOral	Marlex Pharmaceuticals, Inc.	10135-832	10135-0832-0110135-0832-1010135-0832-90
Furosemide	Furosemide 40 mg/1	TabletOral	Marlex Pharmaceuticals, Inc.	10135-833	10135-0833-0110135-0833-1010135-0833-90
Furosemide	Furosemide 80 mg/1	TabletOral	Marlex Pharmaceuticals, Inc.	10135-834	10135-0834-0110135-0834-0510135-0834-90
Furosemide	Furosemide 20 mg/1	TabletOral	Granulation Technology, Inc.	63561-0164	63561-0164-0163561-0164-0263561-0164-09

All 205 Furosemide NDCs

Other NDCs under ANDA 070434

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

FDA NDC Directory listings under ANDA 070434
Product	Strength	Form · route	Labeler	Product NDC
Furosemide	Furosemide 10 mg/mL	SolutionOral	Hikma Pharmaceuticals USA Inc.	0054-3294
Furosemide	Furosemide 40 mg/4mL	SolutionOral	Precision Dose Inc.	68094-756