What is NDC 71335-0273?

71335-0273 is the product NDC for Carvedilol, Carvedilol 25 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 71335-0273 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-0273Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-0273Add 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
71335-0273-1	71335027301	100 TABLET, FILM COATED in 1 BOTTLE (71335-0273-1)Marketed from Sep 6, 2023
71335-0273-2	71335027302	30 TABLET, FILM COATED in 1 BOTTLE (71335-0273-2)Marketed from Mar 30, 2018
71335-0273-3	71335027303	90 TABLET, FILM COATED in 1 BOTTLE (71335-0273-3)Marketed from Jul 2, 2018
71335-0273-4	71335027304	60 TABLET, FILM COATED in 1 BOTTLE (71335-0273-4)Marketed from May 7, 2018
71335-0273-5	71335027305	120 TABLET, FILM COATED in 1 BOTTLE (71335-0273-5)Marketed from Jul 9, 2024
71335-0273-6	71335027306	180 TABLET, FILM COATED in 1 BOTTLE (71335-0273-6)Marketed from Feb 13, 2018
71335-0273-7	71335027307	10 TABLET, FILM COATED in 1 BOTTLE (71335-0273-7)Marketed from Jul 9, 2024

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: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078332
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 71335-0273_ade2e0f6-e1ba-482d-8eb7-df161ee703d7SPL ID ade2e0f6-e1ba-482d-8eb7-df161ee703d7SPL set ID fe4aa7f0-6ef2-4a95-8a64-5e3365f10474RxCUI 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

N471335027301 followed by a unit qualifier and the quantity

Package 71335-0273-01. 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 Jul 9, 2024.

Indications (excerpt from the label)

Carvedilol is 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 to reduce ca…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0273

What is NDC 71335-0273?: 71335-0273 is the product NDC for Carvedilol, Carvedilol 25 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 7 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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 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 3.125 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-499	72888-0499-0172888-0499-0272888-0499-03
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-500	72888-0500-0172888-0500-0272888-0500-03

All 168 Carvedilol NDCs

Other NDCs under ANDA 078332

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

FDA NDC Directory listings under ANDA 078332
Product	Strength	Form · route	Labeler	Product NDC
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-125
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-126
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-129
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-833
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-1069
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-2079
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-409
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-447
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-941
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-946
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-143
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-144
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-145
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-4600
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-132