NDC 0440-1736
Meclizine Hydrochloride 25 mg tablet
On the label: Liberty Pharmaceuticals, 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. 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 Liberty Pharmaceuticals, 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
- Jun 3, 1981
- Package NDCs
0440-1736-08- Official label
- DailyMed (National Library of Medicine), updated Sep 10, 2013
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