NDC 76420-415
Ibuprofen 800 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from SOLA Pharmaceuticals, LLC's NDC 70512-780.
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 SOLA Pharmaceuticals, LLC names for other drugs.
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Ibuprofen: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA078329
- On the market since
- Dec 1, 2024
- Package NDCs
76420-415-0176420-415-0576420-415-3076420-415-6076420-415-90- Official label
- DailyMed (National Library of Medicine), updated Aug 2, 2025
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