Carvedilol NDC 72789-537

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

PD-Rx Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 077614

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 72789-537_5b9fbfaf-db70-04f3-e063-6394a90a4fd8SPL ID 5b9fbfaf-db70-04f3-e063-6394a90a4fd8

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

N472789053790 followed by a unit qualifier and the quantity Copy

Package 72789-0537-90. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 077614

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

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