NDC 61314-238

Carteolol Hydrochloride 10 mg per 1 mL solution

On the label: Sandoz Inc..

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.

Product details

Generic drug
Carteolol: every company that makes it
Form
solution, ophthalmic
Strength
10 mg per 1 mL
Approval
ANDA ANDA075476
On the market since
Jan 5, 2000
Package NDCs
61314-238-05 61314-238-10 61314-238-15
Official label
DailyMed (National Library of Medicine), updated Apr 1, 2025

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