Carvedilol NDC 43063-129

Product information

Brand name (proprietary)

Carvedilol

Generic name (nonproprietary)

carvedilol

Active ingredients

Carvedilol — 25 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

PD-Rx Pharmaceuticals, Inc.

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 43063-129_41378192-7e1a-7f74-e063-6294a90abd88SPL ID 41378192-7e1a-7f74-e063-6294a90abd88SPL set ID 205da5d0-05d9-440d-bb5a-b30b826900abRxCUI 200033UNII 0K47UL67F2UPC 0343063129937

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

N443063012930 followed by a unit qualifier and the quantity Copy

Package 43063-0129-30. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 078332

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