NDC 67046-703
Gabapentin 400 mg capsule
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. rebottles it from Actavis Pharma, Inc.'s NDC 45963-557.
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 Actavis Pharma, Inc. names for other drugs.
Repackaging site
- Coupler Enterprises, Location not on file · repackages it
Recalls
- Dec 15, 2014 · Class II · Actavis Elizabeth LLC
Failed Capsule/Tablet Specifications: Actavis has received several complaint for clumping and breaking of capsules with some bottles showing popped out bottle bottom (round bottom) and creased labels from one distribution center.
Lots: Lot #s: a) G01889A2 Exp 06/2015, b) G01942A1 Exp 08/2015 - Dec 15, 2014 · Class II · Actavis Elizabeth LLC
Failed Capsule/Tablet Specifications: Actavis has received several complaint for clumping and breaking of capsules with some bottles showing popped out bottle bottom (round bottom) and creased labels from one distribution center.
Lots: Lot #s: a) G01966A1, Exp 10/2015, b) G02004A1, Exp 03/2016
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- capsule
- Strength
- 400 mg
- Approval
- ANDA ANDA075350
- On the market since
- Apr 3, 2018
- Package NDCs
67046-703-30- Official label
- DailyMed (National Library of Medicine), updated Dec 20, 2018
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