NDC 67046-482
Mirtazapine 30 mg tablet
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. rebottles it from Mylan Pharmaceuticals Inc.'s NDC 0378-3530.
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 Mylan Pharmaceuticals Inc. names for other drugs.
Recalls
- Jan 19, 2017 · Class II · Mylan Pharmaceuticals Inc.
Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablet in bottle
Lots: a) 3078937 and 3078938 (NDC 0378-3545-93), exp August 2019 b) 3078937 (NDC 0378-3545-01), exp August 2019 c) 3078936 (0378-3545-05), exp August 2019
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Mirtazapine: every company that makes it
- Form
- tablet
- Strength
- 30 mg
- Approval
- ANDA ANDA076122
- On the market since
- Jun 30, 2010
- Package NDCs
67046-482-30- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2010
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