Bimatoprost 0.3 mg per 1 mL solution/ drops

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Sandoz Inc. names for other drugs.

Recalls

• Oct 17, 2019 · Class III · Sandoz Inc
  Labeling: Incorrect or missing package insert.
  Lots: Lot #s: a) 290635FA, 290635FB, Exp. 11/30/2019; 293230F, Exp. 6/30/2020; 294628F, 301337F, Exp. 11/30/2020; 304451FA, Exp. 1/31/2021. b) 290636FA, 290636FB, 290636FC, Exp. 11/30/2019; 293233FA, 293233FB, Exp. 5/31/2020; 293234FA, 293234FB, Exp. 6/30/2020; 294630F, 301338FA, 301338FB, 309426F, Ex…

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

Product details

Generic drug

Bimatoprost: every company that makes it

Form

solution/ drops, ophthalmic

Strength

0.3 mg per 1 mL

Approval

ANDA ANDA202719

On the market since

Dec 6, 2016

Package NDCs

0781-6206-75 0781-6206-93

Official label

DailyMed (National Library of Medicine), updated Aug 31, 2023

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