What is NDC 63187-517?

63187-517 is the product NDC for Furosemide, Furosemide 20 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 63187. 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?

211 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 63187-517 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-517Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0517Add 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
63187-517-30	63187051730	30 TABLET in 1 BOTTLE (63187-517-30)Marketed from Dec 1, 2018
63187-517-60	63187051760	60 TABLET in 1 BOTTLE (63187-517-60)Marketed from Dec 1, 2018
63187-517-90	63187051790	90 TABLET in 1 BOTTLE (63187-517-90)Marketed from Dec 1, 2018

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): Furosemide
Generic name (nonproprietary): furosemide
Active ingredients: Furosemide — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 63187
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077293
Marketing start: Feb 1, 2006
Listing expires: Dec 31, 2026
Other FDA classes: Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers: Product ID 63187-517_2a96ac85-a5c3-48f0-8ab9-7c57ff793502SPL ID 2a96ac85-a5c3-48f0-8ab9-7c57ff793502SPL set ID ce84359c-2f76-421a-9b2b-79b1c2be2f20RxCUI 310429, 313988UNII 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

N463187051730 followed by a unit qualifier and the quantity

Package 63187-0517-30. 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 Jan 1, 2021.

Indications (excerpt from the label)

INDICATIONS AND USAGE Edema FUROSEMIDE TABLET 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 TABLET is particularly useful when an agent with greater diuretic potential is desired. Hypertension Oral FUROSEMIDE TABLET 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 TABLETS alone.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63187-517

What is NDC 63187-517?: 63187-517 is the product NDC for Furosemide, Furosemide 20 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, 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?: Proficient Rx LP, NDC labeler code 63187. 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?: 211 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	Unit Dose Solutions, Inc.	87441-033	87441-0033-01
Furosemide	Furosemide 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4679	70518-4679-00
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 212 Furosemide NDCs

Other NDCs under ANDA 077293

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

FDA NDC Directory listings under ANDA 077293
Product	Strength	Form · route	Labeler	Product NDC
Furosemide	Furosemide 20 mg/1	TabletOral	Calvin Scott & Co., Inc.	17224-178
Furosemide	Furosemide 40 mg/1	TabletOral	Calvin Scott & Co., Inc.	17224-185
Furosemide	Furosemide 40 mg/1	TabletOral	QPharma Inc	42708-123
Furosemide	Furosemide 20 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-702
Furosemide	Furosemide 40 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-716
Furosemide	Furosemide 80 mg/1	TabletOral	A-S Medication Solutions	50090-2713
Furosemide	Furosemide 40 mg/1	TabletOral	A-S Medication Solutions	50090-3313
Furosemide	Furosemide 20 mg/1	TabletOral	A-S Medication Solutions	50090-5429
Furosemide	Furosemide 40 mg/1	TabletOral	A-S Medication Solutions	50090-5702
Furosemide	Furosemide 40 mg/1	TabletOral	A-S Medication Solutions	50090-6937
Furosemide	Furosemide 20 mg/1	TabletOral	Northwind Health Company, LLC	51655-269
Furosemide	Furosemide 40 mg/1	TabletOral	Northwind Health Company, LLC	51655-517
Furosemide	Furosemide 20 mg/1	TabletOral	DIRECT RX	61919-242
Furosemide	Furosemide 40 mg/1	TabletOral	Direct_Rx	61919-255
Furosemide	Furosemide 40 mg/1	TabletOral	Proficient Rx LP	63187-506
Furosemide	Furosemide 20 mg/1	TabletOral	Proficient Rx LP	63187-739
Furosemide	Furosemide 40 mg/1	TabletOral	Proficient Rx LP	63187-790
Furosemide	Furosemide 20 mg/1	TabletOral	Coupler LLC	67046-0768
Furosemide	Furosemide 80 mg/1	TabletOral	Coupler LLC	67046-1555
Furosemide	Furosemide 20 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-1708

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