NDC 24208-585

Tropicamide 10 mg per 1 mL solution/ drops

On the label: Bausch & Lomb Incorporated.

Where it's made

Recalls

• Jan 18, 2016 · Class III · Bausch & Lomb, Inc.
  Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
  Lots: Lot #:199001, Expiry: 01/2016; Lot #: 222591, Expiry: 04/2016; Lot #: 224491, Expiry: 06/2016; Lot #: 229241, Expiry: 08/2016; Lot #: 232941, Expiry: 11/2016; Lot #: 239921, Expiry: 02/2017; Lot #: 241701, Expiry: 04/2017; Lot #: 246851, Expiry: 07/2017.
• Jan 18, 2016 · Class III · Bausch & Lomb, Inc.
  Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
  Lots: a) Lot #: 232601, Expiry: 01/2016; Lot #: 233471, Expiry: 02/2016; Lot #: 234901, Expiry: 03/2016; Lot #: 238861, Expiry: 04/2016; Lot #: 239781, Expiry: 04/2016; Lot #: 243351, Expiry: 08/2016; Lot #: 244931, Expiry: 09/2016. b) Lot #: 198821, Expiry: 01/2016; Lot #: 198901, Expiry: 01/2016; Lot #…

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

Product details

Generic drug

Tropicamide: every company that makes it

Form

solution/ drops, ophthalmic

Strength

10 mg per 1 mL

Approval

ANDA ANDA040064

On the market since

Jul 27, 1994

Package NDCs

24208-585-59 24208-585-64

Official label

DailyMed (National Library of Medicine), updated Sep 1, 2023

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