What is NDC 70518-0426?

70518-0426 is the product NDC for Carvedilol, Carvedilol 6.25 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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 70518-0426 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-0426Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-0426Add 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
70518-0426-0	7051804260070518042600	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0426-0)Marketed from Apr 17, 2017
70518-0426-1	7051804260170518042601	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0426-1)Marketed from Apr 24, 2017
70518-0426-4	7051804260470518042604	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0426-4)Marketed from Jan 7, 2019

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 — 6.25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077614
Marketing start: Apr 17, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)Adrenergic beta1-Antagonists (Mechanism)Adrenergic beta2-Antagonists (Mechanism)
Identifiers: Product ID 70518-0426_5527bc63-f106-e5ca-e063-6294a90a9dbfSPL ID 5527bc63-f106-e5ca-e063-6294a90a9dbfSPL set ID 683bd1c4-fb9d-46cc-9bd4-6a6e455cadfbRxCUI 200031UNII 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

N470518042600 followed by a unit qualifier and the quantity

Package 70518-0426-00. 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 26, 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 indicated …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-0426

What is NDC 70518-0426?: 70518-0426 is the product NDC for Carvedilol, Carvedilol 6.25 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. It has 3 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?: REMEDYREPACK INC., NDC labeler code 70518. 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 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	NuCare Pharmaceuticals,Inc.	68071-2230
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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