What is NDC 55111-255?

55111-255 is the product NDC for Carvedilol, Carvedilol 25 mg/1 tablet, film coated, listed with the FDA by Dr. Reddy's Laboratories Limited. It has 5 package NDCs, shown above in 10- and 11-digit form.

Dr. Reddy's Laboratories Limited, NDC labeler code 55111. 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 55111-255 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)55111-255Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55111-0255Add 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
55111-255-01	5511102550155111025501	100 TABLET, FILM COATED in 1 BOTTLE (55111-255-01)Marketed from Sep 5, 2007
55111-255-05	5511102550555111025505	500 TABLET, FILM COATED in 1 BOTTLE (55111-255-05)Marketed from Sep 5, 2007
55111-255-10	5511102551055111025510	1000 TABLET, FILM COATED in 1 BOTTLE (55111-255-10)Marketed from Sep 5, 2007
55111-255-30	5511102553055111025530	30 TABLET, FILM COATED in 1 BOTTLE (55111-255-30)Marketed from Sep 5, 2007
55111-255-78	5511102557855111025578	10 BLISTER PACK in 1 CARTON (55111-255-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-255-79)Marketed from Sep 5, 2007

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 — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Dr. Reddy's Laboratories LimitedNDC labeler code 55111
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076649
Marketing start: Sep 5, 2007
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)Adrenergic beta1-Antagonists (Mechanism)Adrenergic beta2-Antagonists (Mechanism)
Identifiers: Product ID 55111-255_31305b0b-ee75-85e9-081c-73d15c0a7b83SPL ID 31305b0b-ee75-85e9-081c-73d15c0a7b83SPL set ID 1e453c21-a8a8-dc54-5591-74c972d41727RxCUI 200031, 200032, 200033, 686924UNII 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

N455111025501 followed by a unit qualifier and the quantity

Package 55111-0255-01. 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 Dec 5, 2018.

Indications (excerpt from the label)

Carvedilol is an alpha/beta-adrenergic blocking agent indicated for the treatment of: Left ventricular dysfunction following myocardial infarction in clinically stable patients ( 1.2 ) Hypertension ( 1.3 ) 1.2 Left Ventricular Dysfunction Following Myocardial Infarction Carvedilol tablets are indicated to reduce cardiovascular mortality in clinically stable patients who have survived the acute phase of a myocardial infarction and have a left ventricular ejection fraction of ≤ 40% (with or without symptomatic heart failure) [see Clinical Studies (14.2) ]. 1.3 Hypertension Carvedilol tablets are indicated for the management of essential hypertension [see Clinical Studies (14.3, 14.4) ]. It can…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55111-255

What is NDC 55111-255?: 55111-255 is the product NDC for Carvedilol, Carvedilol 25 mg/1 tablet, film coated, listed with the FDA by Dr. Reddy's Laboratories Limited. It has 5 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?: Dr. Reddy's Laboratories Limited, NDC labeler code 55111. 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 076649

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

FDA NDC Directory listings under ANDA 076649
Product	Strength	Form · route	Labeler	Product NDC
Carvedilol	Carvedilol 3.125 mg/1	Tablet, Film coatedOral	Dr. Reddy's Laboratories Limited	55111-252
Carvedilol	Carvedilol 6.25 mg/1	Tablet, Film coatedOral	Dr. Reddy's Laboratories Limited	55111-253
Carvedilol	Carvedilol 12.5 mg/1	Tablet, Film coatedOral	Dr. Reddy's Laboratories Limited	55111-254