Atorvastatin Calcium NDC 76420-943

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

Asclemed USA, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 209288

Marketing start

Dec 23, 2018

Listing expires

Dec 31, 2026

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 76420-943_352ed2e2-c7bd-ae21-e063-6394a90ad835SPL ID 352ed2e2-c7bd-ae21-e063-6394a90ad835SPL set ID 60d51f39-8086-4434-affe-88ab8ca0c7e5RxCUI 259255, 617310, 617311, 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

N476420094300 followed by a unit qualifier and the quantity Copy

Package 76420-0943-00. 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

Other NDCs under ANDA 209288

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

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