NDC 43063-897
Nortriptyline Hydrochloride 25 mg capsule
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-4002.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Taro Pharmaceutical Industries Ltd. | Haifa Bay, Israel | Makes it | No problems foundDec 8, 2022 · 7 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Recalls
- Jan 8, 2021 · Class II · Taro Pharmaceuticals U.S.A., Inc.
CGMP deviations.
Lots: AC05096, AC05098, and AC05099; Exp 10/31/2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Nortriptyline: every company that makes it
- Form
- capsule
- Strength
- 25 mg
- Approval
- ANDA ANDA075520
- On the market since
- May 8, 2000
- Package NDCs
43063-897-30- Official label
- DailyMed (National Library of Medicine), updated Mar 25, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?