NDC 10544-109
Amitriptyline Hydrochloride 25 mg tablet, film coated
On the label: Blenheim Pharmacal, Inc.. It's repackaged: Blenheim Pharmacal, Inc. rebottles it from Sandoz Inc.'s NDC 0781-1487.
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.
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
- Strength
- 25 mg
- Approval
- ANDA ANDA085966
- On the market since
- Aug 4, 2010
- Package NDCs
10544-109-30- Official label
- DailyMed (National Library of Medicine), updated Aug 24, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?