Simvastatin NDC 50090-7782

Product information

Brand name (proprietary)

Simvastatin

Generic name (nonproprietary)

simvastatin

Active ingredients

Simvastatin — 40 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

A-S Medication Solutions

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 077691

Marketing start

Dec 20, 2006

Listing expires

Dec 31, 2026

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 50090-7782_e50a7b62-7b70-43a9-801f-b15f7edf3d11SPL ID e50a7b62-7b70-43a9-801f-b15f7edf3d11SPL set ID 658cf877-f7cd-4ec8-84a3-08c27a06ccdaRxCUI 198211UNII AGG2FN16EV

Pharmacologic class

HMG-CoA Reductase Inhibitor

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

N450090778200 followed by a unit qualifier and the quantity Copy

Package 50090-7782-00. 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 077691

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

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