Atorvastatin Calcium NDC 50090-6506

Product information

Brand name (proprietary)

Atorvastatin Calcium

Generic name (nonproprietary)

atorvastatin calcium

Active ingredients

Atorvastatin calcium propylene glycol solvate — 80 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 090548

Marketing start

Aug 1, 2021

Listing expires

Dec 31, 2026

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 50090-6506_318deb0c-d033-4439-bf62-0bacfd6c2d86SPL ID 318deb0c-d033-4439-bf62-0bacfd6c2d86SPL set ID 77675dc3-868d-42a3-a179-80372a23e0c8RxCUI 259255UNII YRZ789OWMI

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

N450090650600 followed by a unit qualifier and the quantity Copy

Package 50090-6506-00. 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 090548

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

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