What is NDC 23155-871?

23155-871 is the product NDC for Torsemide, Torsemide 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.

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 Torsemide?

60 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Torsemide NDC 23155-871 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)23155-871Labeler and product segments. Claims need a package NDC.

Product NDC at billing width23155-0871Add 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
23155-871-01	2315508710123155087101	100 TABLET in 1 BOTTLE (23155-871-01)Marketed from Jul 24, 2023
23155-871-05	2315508710523155087105	500 TABLET in 1 BOTTLE (23155-871-05)Marketed from Jul 24, 2023
23155-871-10	2315508711023155087110	1000 TABLET in 1 BOTTLE (23155-871-10)Marketed from Jul 24, 2023

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): Torsemide
Generic name (nonproprietary): torsemide
Active ingredients: Torsemide — 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 076894
Marketing start: Jul 24, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers: Product ID 23155-871_98d688f8-ec71-4b98-86b8-d405bdffc4c3SPL ID 98d688f8-ec71-4b98-86b8-d405bdffc4c3SPL set ID 03fbbb85-4e0f-4f3b-b4b0-87f84cb33d47RxCUI 198369, 198370, 198371, 198372UNII W31X2H97FBUPC 0323155873016
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

N423155087101 followed by a unit qualifier and the quantity

Package 23155-0871-01. 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 30, 2023.

Indications (excerpt from the label)

Torsemide is a loop diuretic indicated for: the treatment of edema associated with heart failure, renal disease or hepatic disease. ( 1.1 ) the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.2 ) 1.1 Edema Torsemide tablets are indicated for the treatment of edema associated with heart failure, renal disease or hepatic disease. 1.2 Hypertension Torsemide tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial in…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23155-871

What is NDC 23155-871?: 23155-871 is the product NDC for Torsemide, Torsemide 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?: Torsemide.
What is the active ingredient?: Torsemide.
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 Torsemide?: 60 other product NDCs are listed under this name. See all Torsemide 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 Torsemide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Torsemide	Torsemide 5 mg/1	TabletOral	XLCare Pharmaceuticals Inc.	72865-258	72865-0258-90
Torsemide	Torsemide 10 mg/1	TabletOral	XLCare Pharmaceuticals Inc.	72865-259	72865-0259-0172865-0259-90
Torsemide	Torsemide 20 mg/1	TabletOral	XLCare Pharmaceuticals Inc.	72865-260	72865-0260-0172865-0260-0572865-0260-90
Torsemide	Torsemide 100 mg/1	TabletOral	XLCare Pharmaceuticals Inc.	72865-261	72865-0261-0172865-0261-90
Torsemide	Torsemide 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4139	70518-4139-00
Torsemide	Torsemide 10 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-872	23155-0872-0123155-0872-0523155-0872-10
Torsemide	Torsemide 20 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-873	23155-0873-0123155-0873-0523155-0873-10
Torsemide	Torsemide 100 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-874	23155-0874-0123155-0874-0523155-0874-10
Torsemide	Torsemide 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-2663	71335-2663-0171335-2663-02
Torsemide	Torsemide 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-2841	71335-2841-01

All 61 Torsemide NDCs

Other NDCs under ANDA 076894

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

FDA NDC Directory listings under ANDA 076894
Product	Strength	Form · route	Labeler	Product NDC
Torsemide	Torsemide 10 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-872
Torsemide	Torsemide 20 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-873
Torsemide	Torsemide 100 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-874
Torsemide	Torsemide 5 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-596
Torsemide	Torsemide 10 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-597
Torsemide	Torsemide 100 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-598
Torsemide	Torsemide 5 mg/1	TabletOral	Chartwell RX, LLC	62135-818
Torsemide	Torsemide 10 mg/1	TabletOral	Chartwell RX, LLC	62135-819
Torsemide	Torsemide 20 mg/1	TabletOral	Chartwell RX, LLC	62135-820
Torsemide	Torsemide 100 mg/1	TabletOral	Chartwell RX, LLC	62135-821
Torsemide	Torsemide 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4139
Torsemide	Torsemide 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-2663
Torsemide	Torsemide 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-2841
Torsemide	Torsemide 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-2962
Torsemide	Torsemide 20 mg/1	TabletOral	Bryant Ranch Prepack	72162-2412