NDC 53808-1116
Meclizine Hydrochloride 25 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 59746-121, made by Jubilant Cadista Pharmacuticals 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). 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 State of Florida DOH Central Pharmacy names for other drugs.
Product details
- Generic drug
- Meclizine: every company that makes it
- Form
- tablet
- Strength
- 25 mg
- Approval
- ANDA ANDA040659
- On the market since
- Oct 26, 2017
- Package NDCs
53808-1116-1- Official label
- DailyMed (National Library of Medicine), updated Jan 18, 2019
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