Taro Pharmaceutical Industries Ltd.
Haifa Bay, Israel · makes it
No problems found Last FDA inspection Dec 8, 2022. 7 inspections on record.
NDC 50436-4022
Nortriptyline Hydrochloride 25 mg capsule
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-4002.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Recalls
- Jan 8, 2021 · Class II · Terminated
CGMP deviations.
Lots: AC05096, AC05098, and AC05099; Exp 10/31/2022
Product details
- Generic drug
- Nortriptyline: see every company that makes it
- Form
- capsule
- Strength
- 25 mg
- Approval
- ANDA ANDA075520
- On the market since
- May 8, 2000
- Package NDCs
50436-4022-2- Official label
- DailyMed (National Library of Medicine), updated Apr 19, 2018
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