What is NDC 50090-7704?

50090-7704 is the product NDC for Furosemide, Furosemide 40 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.

A-S Medication Solutions, NDC labeler code 50090. 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 50090-7704 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-7704Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-7704Add 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
50090-7704-1	5009077040150090770401	180 TABLET in 1 BOTTLE (50090-7704-1)Marketed from Oct 14, 2025

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 — 40 mg/1
Dosage form: Tablet
Route: Oral
Labeler: A-S Medication SolutionsNDC labeler code 50090
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078010
Marketing start: Jun 3, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers: Product ID 50090-7704_1839739b-7e49-4a30-8305-a32ae079735aSPL ID 1839739b-7e49-4a30-8305-a32ae079735aSPL set ID c81d313c-65a3-4fb5-b6cd-b1c1ec7dca03RxCUI 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

N450090770401 followed by a unit qualifier and the quantity

Package 50090-7704-01. 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.

About NDC 50090-7704

What is NDC 50090-7704?: 50090-7704 is the product NDC for Furosemide, Furosemide 40 mg/1 tablet, listed with the FDA by A-S Medication Solutions. 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?: A-S Medication Solutions, NDC labeler code 50090. 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 078010

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

FDA NDC Directory listings under ANDA 078010
Product	Strength	Form · route	Labeler	Product NDC
Furosemide	Furosemide 40 mg/1	TabletOral	A-S Medication Solutions	50090-7703
Furosemide	Furosemide 40 mg/1	TabletOral	A-S Medication Solutions	50090-7705
Furosemide	Furosemide 20 mg/1	TabletOral	A-S Medication Solutions	50090-7706
Furosemide	Furosemide 20 mg/1	TabletOral	A-S Medication Solutions	50090-7708
Furosemide	Furosemide 20 mg/1	TabletOral	Coupler LLC	67046-1589
Furosemide	Furosemide 40 mg/1	TabletOral	Coupler LLC	67046-1663
Furosemide	Furosemide 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4679
Furosemide	Furosemide 20 mg/1	TabletOral	Ipca Laboratories Limited	83980-002
Furosemide	Furosemide 40 mg/1	TabletOral	Ipca Laboratories Limited	83980-003
Furosemide	Furosemide 80 mg/1	TabletOral	Ipca Laboratories Limited	83980-004