What is NDC 72888-501?

72888-501 is the product NDC for Carvedilol, Carvedilol 12.5 mg/1 tablet, film coated, listed with the FDA by Advagen Pharma Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.

Advagen Pharma Limited, NDC labeler code 72888. 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 72888-501 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72888-501Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72888-0501Add 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
72888-501-01	7288805010172888050101	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72888-501-01)Marketed from Sep 17, 2025
72888-501-02	7288805010272888050102	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72888-501-02)Marketed from Sep 17, 2025
72888-501-03	7288805010372888050103	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72888-501-03)Marketed from Sep 17, 2025

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 — 12.5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Advagen Pharma LimitedNDC labeler code 72888
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078786
Marketing start: Sep 17, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)Adrenergic beta1-Antagonists (Mechanism)Adrenergic beta2-Antagonists (Mechanism)
Identifiers: Product ID 72888-501_4b7daf77-d3f7-0b55-e063-6394a90a84fcSPL ID 4b7daf77-d3f7-0b55-e063-6394a90a84fcSPL set ID 205291ba-86a7-43e1-be47-bc75df1921f9RxCUI 200031, 200032, 200033, 686924UNII 0K47UL67F2UPC 0372888501031, 0372888501024, 0372888500027, 0372888499031, 0372888502021, 0372888502038, 0372888501017, 0372888502014
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

N472888050101 followed by a unit qualifier and the quantity

Package 72888-0501-01. 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 23, 2026.

Indications (excerpt from the label)

Carvedilol tablets, USP 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, USP 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, USP are in…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72888-501

What is NDC 72888-501?: 72888-501 is the product NDC for Carvedilol, Carvedilol 12.5 mg/1 tablet, film coated, listed with the FDA by Advagen Pharma Limited. 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?: Advagen Pharma Limited, NDC labeler code 72888. 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 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 170 Carvedilol NDCs

Other NDCs under ANDA 078786

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

FDA NDC Directory listings under ANDA 078786
Product	Strength	Form · route	Labeler	Product NDC
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Method Pharmaceuticals, LLC	58657-750
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Method Pharmaceuticals, LLC	58657-751
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Method Pharmaceuticals, LLC	58657-752
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Method Pharmaceuticals, LLC	58657-753
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-499
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-500
Carvedilol	Carvedilol 25 mg/1	Tablet, Film coatedOral	Advagen Pharma Limited	72888-502