NDC 82868-086
Amitriptyline Hydrochloride 50 mg tablet, film coated
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Sandoz Inc.'s NDC 0781-1488.
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 Sandoz Inc. names for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Jun 16, 2017 · Class III · Sandoz Incorporated
Cross Contamination With Other Product: Imipramine
Lots: Lot #: a) GR3831, GS9690, Exp. 08/2019; b) GR3832, Exp. 08/2019.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Amitriptyline: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA085968
- On the market since
- Aug 21, 2025
- Package NDCs
82868-086-90- Official label
- DailyMed (National Library of Medicine), updated Dec 29, 2025
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