NDC 31722-778

Acyclovir 800 mg tablet

On the label: Camber Pharmaceuticals Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Hetero Labs LimitedMahabubnagar, IndiaMakes it Problems found, fixed voluntarilyAug 12, 2022 · 5 inspections, 1 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Acyclovir: every company that makes it
Form
tablet, oral
Strength
800 mg
Approval
ANDA ANDA203834
On the market since
Nov 29, 2013
Package NDCs
31722-778-01 31722-778-05
Official label
DailyMed (National Library of Medicine), updated Feb 2, 2026

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