NDC 73614-201
Ibuprofen 800 mg tablet, film coated
On the label: Brisk Pharmaceuticals, Inc.. It's repackaged: Brisk Pharmaceuticals, Inc. rebottles it from Westminster Pharmaceuticals, LLC's NDC 69367-396.
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 Westminster Pharmaceuticals, LLC names for other drugs.
Product details
- Generic drug
- Ibuprofen: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA202413
- On the market since
- May 23, 2024
- Package NDCs
73614-201-03- Official label
- DailyMed (National Library of Medicine), updated Feb 10, 2025
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