NDC 71921-146

Acyclovir 200 mg capsule

On the label: Florida Pharmaceutical Products, LLC..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Contract Pharmacal Corp.Hauppauge, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyApr 14, 2022 · 13 inspections, 1 with FDA action

Product details

Generic drug
Acyclovir: every company that makes it
Form
capsule, oral
Strength
200 mg
Approval
ANDA ANDA075090
On the market since
Feb 18, 2026
Package NDCs
71921-146-01
Official label
DailyMed (National Library of Medicine), updated Feb 18, 2026

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