NDC 0065-0817

atropine sulfate 10 mg per 1 mL solution

On the label: Alcon Laboratories, Inc..

United States: 1Germany: 1India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Alcon Research LLCFort Worth, TX, United StatesMakes it No problems foundSep 15, 2022 · 12 inspections
Boehringer Ingelheim Pharma GmbH and Co. KGIngelheim am Rhein, GermanyMakes the active ingredient and tests it Problems found, fixed voluntarilyMay 15, 2025 · 8 inspections, 1 with FDA action
Laurus Labs LimitedAnakapalli, IndiaMakes the active ingredient and tests it No problems foundApr 19, 2024 · 6 inspections

Product details

Generic drug
Atropine: every company that makes it
Form
solution, ophthalmic
Strength
10 mg per 1 mL
Approval
NDA NDA208151
On the market since
Nov 1, 2022
Package NDCs
0065-0817-01 0065-0817-02
Official label
DailyMed (National Library of Medicine), updated Mar 13, 2026

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