Metoprolol Tartrate NDC 71335-9745

Product information

Brand name (proprietary)

Metoprolol Tartrate

Generic name (nonproprietary)

metoprolol tartrate

Active ingredients

Metoprolol tartrate — 25 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 200981

Marketing start

Dec 1, 2018

Listing expires

Dec 31, 2027

Other FDA classes

Adrenergic beta-Antagonists (Mechanism)

Identifiers

Product ID 71335-9745_44a48f7d-3c83-49bb-b471-cf858db52117SPL ID 44a48f7d-3c83-49bb-b471-cf858db52117SPL set ID 840ac287-cae5-4c07-82d5-546fb04414efRxCUI 866924UNII W5S57Y3A5L

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

N471335974501 followed by a unit qualifier and the quantity Copy

Package 71335-9745-01. 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

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

Other NDCs under ANDA 200981

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

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