NDC 68071-2408

Acyclovir 800 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Carlsbad Technology, Inc.'s NDC 61442-113.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Carlsbad Technology, Inc.Carlsbad, CA, United StatesMakes it and tests it Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections

Repackaging site

Product details

Generic drug
Acyclovir: every company that makes it
Form
tablet, oral
Strength
800 mg
Approval
ANDA ANDA075382
On the market since
Oct 22, 2009
Package NDCs
68071-2408-1 68071-2408-2 68071-2408-3 68071-2408-4 68071-2408-5 68071-2408-7
Official label
DailyMed (National Library of Medicine), updated Mar 26, 2026

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