NDC 76420-182
Lamotrigine 200 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 29300-114.
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 Unichem Pharmaceuticals (USA), Inc. names for other drugs.
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · relabels it
Recalls
- Aug 19, 2016 · Class III · Unichem Pharmaceuticals Usa Inc
Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the tablets.
Lots: Lot #: GLEH 16003, Exp 03/31/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Lamotrigine: every company that makes it
- Form
- tablet, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA090170
- On the market since
- Nov 1, 2011
- Package NDCs
76420-182-60- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2020
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