NDC 53217-372

Ranitidine 300 mg tablet, film coated

On the label: Aidarex Pharmaceuticals LLC. It's repackaged from NDC 68462-249, made by Glenmark Pharmaceuticals Inc., USA (Ranitidine). That product's FDA listing has since ended, so its label and factories are no longer published.

Where the pills inside were made

This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 Aidarex Pharmaceuticals LLC names for other drugs.

Product details

Generic drug
Ranitidine: every company that makes it
Form
tablet, film coated
Strength
300 mg
Approval
ANDA ANDA078542
On the market since
Apr 9, 2018
Package NDCs
53217-372-30
Official label
DailyMed (National Library of Medicine), updated Aug 23, 2018

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