NDC 49349-218
Loratadineantihistamineantihistamine 10 mg tablet
On the label: Remedyrepack Inc.. It's repackaged from NDC 45802-650, made by Padagis Israel Pharmaceuticals Ltd (Loratadine). 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 Remedyrepack Inc. names for other drugs.
Product details
- Generic drug
- Loratadine: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA076301
- On the market since
- May 20, 2013
- Package NDCs
49349-218-20- Official label
- DailyMed (National Library of Medicine), updated May 20, 2013
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