Metoprolol Tartrate (metoprolol) NDC 60760-944

Product information

Brand name (proprietary)

Metoprolol Tartrate

Generic name (nonproprietary)

metoprolol

Active ingredients

Metoprolol tartrate — 50 mg/1

Dosage form

Tablet

Route

Oral

Labeler

St. Mary's Medical Park Pharmacy

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 202871

Marketing start

Sep 11, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Adrenergic beta-Antagonists (Mechanism)

Identifiers

Product ID 60760-944_5b867129-3b86-f12c-e063-6294a90ac407SPL ID 5b867129-3b86-f12c-e063-6294a90ac407

Pharmacologic class

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

N460760094460 followed by a unit qualifier and the quantity Copy

Package 60760-0944-60. 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 202871

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