NDC 82804-971

AMLODIPINE BESYLATE10 mg 10 mg tablet

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-023.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Oxford Pharmaceuticals, LLCBirmingham, AL, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections

Repackaging site

Product details

Generic drug
Amlodipine: every company that makes it
Form
tablet, oral
Strength
10 mg
Approval
ANDA ANDA078414
On the market since
Oct 1, 2021
Package NDCs
82804-971-00 82804-971-11 82804-971-30 82804-971-55 82804-971-60 82804-971-72 82804-971-90
Official label
DailyMed (National Library of Medicine), updated Feb 1, 2025

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