NDC 67296-1339
Ibuprofen 600 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Bi-Coastal Pharma International LLC's NDC 42582-112.
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 Bi-Coastal Pharma International LLC names for other drugs.
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it and relabels it
Recalls
- Jan 11, 2018 · Class II · Time-Cap Laboratories, Inc.
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Lots: a) D044C, D038C, D043C, exp 3/18, b) C136C, exp 3/18, D039C, D040C, D041C, D042C, 3/18 - Jan 11, 2018 · Class II · Time-Cap Laboratories, Inc.
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Lots: a) C135C, exp 3/18 b) C134C, exp 3/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ibuprofen: every company that makes it
- Form
- tablet
- Strength
- 600 mg
- Approval
- ANDA ANDA090796
- On the market since
- Apr 14, 2016
- Package NDCs
67296-1339-167296-1339-3- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2020
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