NDC 10544-108

Meclizine Hydrochloride 25 mg tablet

On the label: Blenheim Pharmacal, Inc.. It's repackaged from NDC 49884-035, made by Par Pharmaceutical, Inc. (Meclizine Hydrochloride). 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 and relabels 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 Blenheim Pharmacal, Inc. names for other drugs.

Product details

Generic drug
Meclizine: every company that makes it
Form
tablet
Strength
25 mg
Approval
ANDA ANDA087128
On the market since
Dec 16, 2009
Package NDCs
10544-108-15 10544-108-20 10544-108-30
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2014

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