NDC 61314-637

Prednisolone Acetate 10 mg per 1 mL suspension/ drops

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.

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
Prednisolone: every company that makes it
Form
suspension/ drops, ophthalmic
Strength
10 mg per 1 mL
Approval
NDA authorized generic NDA017469
On the market since
Dec 15, 1994
Package NDCs
61314-637-05 61314-637-10 61314-637-15
Official label
DailyMed (National Library of Medicine), updated Dec 30, 2024

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