What is NDC 68071-2230?

68071-2230 is the product NDC for Carvedilol, Carvedilol 12.5 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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 68071-2230 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-2230Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-2230Add 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
68071-2230-3	6807122300368071223003	180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-3)Marketed from Jan 2, 2025
68071-2230-6	6807122300668071223006	60 TABLET, FILM COATED in 1 BOTTLE (68071-2230-6)Marketed from Aug 4, 2020
68071-2230-8	6807122300868071223008	180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-8)Marketed from Aug 4, 2020
68071-2230-9	6807122300968071223009	90 TABLET, FILM COATED in 1 BOTTLE (68071-2230-9)Marketed from Aug 4, 2020

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): Carvedilol
Generic name (nonproprietary): carvedilol
Active ingredients: Carvedilol — 12.5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077614
Marketing start: Sep 5, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)Adrenergic beta1-Antagonists (Mechanism)Adrenergic beta2-Antagonists (Mechanism)
Identifiers: Product ID 68071-2230_2ac0f53e-48b2-5d84-e063-6294a90a8ac8SPL ID 2ac0f53e-48b2-5d84-e063-6294a90a8ac8SPL set ID ac14846e-423a-37c4-e053-2a95a90a3cddRxCUI 200032UNII 0K47UL67F2UPC 0368071223095
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

N468071223003 followed by a unit qualifier and the quantity

Package 68071-2230-03. 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 2, 2025.

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 ) and Clinical Studies ( 14.1 ) ]. 1.2 Left Ventricular Dysfunction following Myocardial Infarction Carvedilol tablets are indica…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68071-2230

What is NDC 68071-2230?: 68071-2230 is the product NDC for Carvedilol, Carvedilol 12.5 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 4 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?: NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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 077614

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

FDA NDC Directory listings under ANDA 077614
Product	Strength	Form · route	Labeler	Product NDC
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-2780
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-582
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-1826
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-411
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-0356
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-0426
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-4060
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-4070
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0336
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-029
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-030
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-034
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-1067
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-1062
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals, Inc.	68071-3138
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-0840
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-6878
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2101
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8252
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-2389

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