NDC 68071-2222

Prednisolone Acetate 10 mg per 1 mL suspension/ drops

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Pacific Pharma, Inc.'s NDC 60758-119.

Where the pills inside were 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 Pacific Pharma, Inc. names for other drugs.

Repackaging site

Product details

Generic drug
Prednisolone: every company that makes it
Form
suspension/ drops, ophthalmic
Strength
10 mg per 1 mL
Approval
NDA authorized generic NDA017011
On the market since
Aug 19, 1997
Package NDCs
68071-2222-5
Official label
DailyMed (National Library of Medicine), updated Jul 17, 2024

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