Atorvastatin Calcium NDC 55154-4384

Product information

Brand name (proprietary)

Atorvastatin Calcium

Generic name (nonproprietary)

atorvastatin calcium

Active ingredients

Atorvastatin calcium trihydrate — 80 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Cardinal Health 107, LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 091226

Marketing start

Jan 23, 2014

Marketing end

Feb 28, 2027

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 55154-4384_befe2578-33dc-43ca-85b4-3b2eed25cdb0SPL ID befe2578-33dc-43ca-85b4-3b2eed25cdb0SPL set ID aee307d6-b3fa-424f-8656-1f30ff413e95RxCUI 259255UNII 48A5M73Z4Q

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

N455154438406 followed by a unit qualifier and the quantity Copy

Package 55154-4384-06. 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 091226

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