Metoprolol succinate NDC 71335-9706

Product information

Brand name (proprietary)

Metoprolol succinate

Generic name (nonproprietary)

metoprolol succinate

Active ingredients

Metoprolol succinate — 100 mg/1

Dosage form

Tablet, Extended release

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 213854

Marketing start

Apr 29, 2021

Listing expires

Dec 31, 2026

Other FDA classes

Adrenergic beta-Antagonists (Mechanism)

Identifiers

Product ID 71335-9706_efb80d5c-17bc-47c0-a6ef-b2b5995519eaSPL ID efb80d5c-17bc-47c0-a6ef-b2b5995519eaSPL set ID 6103540c-93b5-46e8-9ef3-5059fa0335abRxCUI 866412UNII TH25PD4CCB

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

N471335970601 followed by a unit qualifier and the quantity Copy

Package 71335-9706-01. 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

Other NDCs under ANDA 213854

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