What is NDC 68788-9265?

68788-9265 is the product NDC for Carvedilol, Carvedilol 25 mg/1 tablet, film coated, listed with the FDA by Preferred Pharmaceuticals,Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

Preferred Pharmaceuticals,Inc., NDC labeler code 68788. 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?

167 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 68788-9265 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-9265Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-9265Add 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
68788-9265-1	68788926501	100 TABLET, FILM COATED in 1 BOTTLE (68788-9265-1)Marketed from Dec 3, 2014
68788-9265-3	68788926503	30 TABLET, FILM COATED in 1 BOTTLE (68788-9265-3)Marketed from Dec 3, 2014
68788-9265-6	68788926506	60 TABLET, FILM COATED in 1 BOTTLE (68788-9265-6)Marketed from Dec 3, 2014
68788-9265-9	68788926509	90 TABLET, FILM COATED in 1 BOTTLE (68788-9265-9)Marketed from Dec 3, 2014

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 — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Preferred Pharmaceuticals,Inc.NDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077614
Marketing start: Dec 3, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)Adrenergic beta1-Antagonists (Mechanism)Adrenergic beta2-Antagonists (Mechanism)
Identifiers: Product ID 68788-9265_8cbf4bb1-72f2-4e70-9a43-ba62d8fb3317SPL ID 8cbf4bb1-72f2-4e70-9a43-ba62d8fb3317SPL set ID 81bc612d-5674-45b9-a1f5-2cb4fa625747RxCUI 200031, 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

N468788926501 followed by a unit qualifier and the quantity

Package 68788-9265-01. 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 Feb 14, 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 ), Clinical Studies ( 14.1 )] . 1.2 Left Ventricular Dysfunction following Myocardial Infarction Carvedilol tablets are indi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-9265

What is NDC 68788-9265?: 68788-9265 is the product NDC for Carvedilol, Carvedilol 25 mg/1 tablet, film coated, listed with the FDA by Preferred 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?: Preferred Pharmaceuticals,Inc., NDC labeler code 68788. 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?: 167 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 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 6.25 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-500	72888-0500-0172888-0500-0272888-0500-03
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-499	72888-0499-0172888-0499-0272888-0499-03
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-501	72888-0501-0172888-0501-0272888-0501-03

All 168 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 12.5 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-6878
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0879
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-1623
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-411
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0973
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7786
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals,Inc.	68788-9789
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-5726
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4389
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-4956
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-397
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-6949
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-494
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	65841-616
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-4171
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-570
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	65841-617
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	65841-618
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	65841-619
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-2780

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