NDC 71205-911
Clomipramine Hydrochloride 50 mg capsule
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Leading Pharma, LLC's NDC 69315-166.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Leading Pharma, LLC | Fairfield, NJ, United States | Makes it | Problems found, fixed voluntarilyOct 21, 2024 · 13 inspections |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Recalls
- Aug 23, 2022 · Class III · Leading Pharma, LLC
Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules
Lots: Lot#: B14221, Exp. Date 02/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Clomipramine: every company that makes it
- Form
- capsule, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA211364
- On the market since
- Mar 10, 2020
- Package NDCs
71205-911-0071205-911-1171205-911-3071205-911-5571205-911-6071205-911-90- Official label
- DailyMed (National Library of Medicine), updated Apr 1, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?