NDC 0463-6352
Amitriptyline Hydrochloride 50 mg tablet, film coated
On the label: C.O. Truxton, Inc.. It's repackaged from NDC 0603-2214, made by Par Pharmaceutical, Inc. (Amitriptyline Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 C.O. Truxton, Inc. names for other drugs.
Recalls
- Apr 20, 2017 · Class II · C. O. Truxton
Labeling: Label Mixup; potentially mislabeled
Lots: Lot # C0260416A; Exp. 03/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Amitriptyline: every company that makes it
- Form
- tablet, film coated
- Strength
- 50 mg
- Approval
- ANDA ANDA040218
- On the market since
- Sep 11, 1997
- Package NDCs
0463-6352-01- Official label
- DailyMed (National Library of Medicine), updated Jun 5, 2014
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?