NDC 67296-1849
Meclizine Hydrochloride 25 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged from NDC 62559-842, made by ANI Pharmaceuticals, 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 RedPharm Drug. Inc. names for other drugs.
Product details
- Generic drug
- Meclizine: every company that makes it
- Form
- tablet
- Strength
- 25 mg
- Approval
- ANDA ANDA084657
- On the market since
- Dec 27, 2021
- Package NDCs
67296-1849-3- Official label
- DailyMed (National Library of Medicine), updated Feb 7, 2023
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