NDC 75834-256

Atorvastatin calcium 20 mg tablet

On the label: Pharmaceutical Associates, Inc..

Where it's made

Umedica Laboratories Private Limited

Vapi, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Mar 29, 2024. 4 inspections on record.

Product details

Generic drug

Atorvastatin: see every company that makes it

Form

tablet, oral

Strength

20 mg

Approval

ANDA ANDA213853

On the market since

Aug 26, 2020

Package NDCs

75834-256-01 75834-256-05 75834-256-50 75834-256-90

Official label

DailyMed (National Library of Medicine), updated Oct 23, 2026

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