What is NDC 51655-033?

51655-033 is the product NDC for Carvedilol, Carvedilol 25 mg/1 tablet, film coated, listed with the FDA by Northwind Health Company, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Northwind Health Company, LLC, NDC labeler code 51655. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Carvedilol?

169 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Carvedilol NDC 51655-033 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51655-033Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51655-0033Add 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
51655-033-25	5165500332551655003325	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-033-25)Marketed from Jan 20, 2022
51655-033-26	5165500332651655003326	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-033-26)Marketed from Sep 29, 2020

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): Carvedilol
Generic name (nonproprietary): carvedilol
Active ingredients: Carvedilol — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Northwind Health Company, LLCNDC labeler code 51655
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078251
Marketing start: Sep 29, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)Adrenergic beta1-Antagonists (Mechanism)Adrenergic beta2-Antagonists (Mechanism)
Identifiers: Product ID 51655-033_4aa4918b-13cb-07a6-e063-6394a90aa6e8SPL ID 4aa4918b-13cb-07a6-e063-6394a90aa6e8SPL set ID c133b9c7-ab1a-e517-e053-2995a90a517aRxCUI 200033UNII 0K47UL67F2
Pharmacologic class: alpha-Adrenergic Blocker; beta-Adrenergic Blocker

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

N451655003325 followed by a unit qualifier and the quantity

Package 51655-0033-25. 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, 2026.

Indications (excerpt from the label)

Carvedilol tablets are an alpha-/beta-adrenergic blocking agent indicated for the treatment of: mild to severe chronic heart failure ( 1.1 ) left ventricular dysfunction following myocardial infarction in clinically stable patients ( 1.2 ) hypertension ( 1.3 ) 1.1 Heart Failure Carvedilol tablets are indicated for the treatment of mild-to-severe chronic heart failure of ischemic or cardiomyopathic origin, usually in addition to diuretics, ACE inhibitors, and digitalis, to increase survival and, also, to reduce the risk of hospitalization [see Drug Interactions ( 7.4 ), Clinical Studies ( 14.1 )]. 1.2 Left Ventricular Dysfunction following Myocardial Infarction Carvedilol tablets are indicate…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51655-033

What is NDC 51655-033?: 51655-033 is the product NDC for Carvedilol, Carvedilol 25 mg/1 tablet, film coated, listed with the FDA by Northwind Health Company, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Carvedilol.
What is the active ingredient?: Carvedilol.
Who is the labeler?: Northwind Health Company, LLC, NDC labeler code 51655. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Carvedilol?: 169 other product NDCs are listed under this name. See all Carvedilol 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 Carvedilol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-690	72189-0690-90
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0973	67046-0973-03
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0879	67046-0879-03
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0336	67046-0336-03
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-664	72189-0664-60
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-663	72189-0663-90
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-653	72189-0653-90
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1616	67046-1616-03
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-501	72888-0501-0172888-0501-0272888-0501-03
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-499	72888-0499-0172888-0499-0272888-0499-03

All 170 Carvedilol NDCs

Other NDCs under ANDA 078251

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

FDA NDC Directory listings under ANDA 078251
Product	Strength	Form · route	Labeler	Product NDC
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7305
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7306
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7307
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7308
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-2119
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-2175
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-4898
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-6865
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-2640
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-2641
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-2648
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-2649
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-131
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Redpharm Drug	67296-2298
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-2773
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-4816
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Glenmark Pharmaceuticals Inc., USA	68462-162
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Glenmark Pharmaceuticals Inc., USA	68462-163
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Glenmark Pharmaceuticals Inc., USA	68462-164
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Glenmark Pharmaceuticals Inc., USA	68462-165

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