Atorvastatin Calcium NDC 71335-9723

Product information

Brand name (proprietary)

Atorvastatin Calcium

Generic name (nonproprietary)

atorvastatin calcium

Active ingredients

Atorvastatin calcium trihydrate — 40 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 214659

Marketing start

Aug 29, 2022

Listing expires

Dec 31, 2026

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 71335-9723_6b6c1e31-f207-400f-9599-a2f96c5bb3c7SPL ID 6b6c1e31-f207-400f-9599-a2f96c5bb3c7SPL set ID a20bac35-a3d7-4e97-95c2-2502107d61c2RxCUI 617311UNII 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

N471335972301 followed by a unit qualifier and the quantity Copy

Package 71335-9723-01. 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 214659

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