Atorvastatin Calcium NDC 43063-496

Product information

Brand name (proprietary)

Atorvastatin Calcium

Generic name (nonproprietary)

atorvastatin calcium

Active ingredients

Atorvastatin calcium propylene glycol solvate — 20 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

PD-Rx Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 090548

Marketing start

May 29, 2012

Listing expires

Dec 31, 2027

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 43063-496_5c2c31b6-62a4-b918-e063-6294a90ad2f2SPL ID 5c2c31b6-62a4-b918-e063-6294a90ad2f2

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

N443063049630 followed by a unit qualifier and the quantity Copy

Package 43063-0496-30. 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

The FDA listing for this product does not reference a label (SPL) set.

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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