Atorvastatin calcium NDC 67046-1491

Product information

Brand name (proprietary)

Atorvastatin calcium

Generic name (nonproprietary)

atorvastatin calcium

Active ingredients

Atorvastatin calcium trihydrate — 10 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Coupler LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 217081

Marketing start

Jan 29, 2025

Listing expires

Dec 31, 2026

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 67046-1491_2cd99334-31e3-10ef-e063-6294a90acc1eSPL ID 2cd99334-31e3-10ef-e063-6294a90acc1eSPL set ID 2cd9999b-e18f-09de-e063-6294a90a108bRxCUI 617312UNII 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

N467046149103 followed by a unit qualifier and the quantity Copy

Package 67046-1491-03. 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 217081

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