NDC 53002-2091

Amoxicillin 250 mg per 5 mL powder, for suspension

On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-4155.

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 Teva Pharmaceuticals USA, Inc. names for other drugs.

Repackaging site

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
Amoxicillin: every company that makes it
Form
powder, for suspension
Strength
250 mg per 5 mL
Approval
ANDA ANDA061931
On the market since
Sep 30, 1990
Package NDCs
53002-2091-1 53002-2091-2 53002-2091-3
Official label
DailyMed (National Library of Medicine), updated Jun 7, 2023

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