NDC 68151-0149
Ethambutol Hydrochloride 100 mg tablet
On the label: Carilion Materials Management. It's repackaged: Carilion Materials Management rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-280.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
| Lupin Limited | Nagpur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Repackaging site
- Carilion Materials Management, Roanoke, Virginia, United States · repackages it
Recalls
- Feb 22, 2013 · Class III · Lupin Pharmaceuticals Inc.
Failed Impurities/Degradation Specifications: This product is being recalled due to an out of specification result for an impurity.
Lots: Lot #: 3122856, Exp 05/14
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ethambutol: every company that makes it
- Form
- tablet
- Strength
- 100 mg
- Approval
- ANDA ANDA078939
- On the market since
- Jul 4, 2009
- Package NDCs
68151-0149-0- Official label
- DailyMed (National Library of Medicine), updated Jul 6, 2017
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