NDC 50090-3282
Phentermine 15 mg capsule
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Aurolife Pharma LLC's NDC 13107-105.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
| Aurolife Pharma LLC | Dayton, NJ, United States | Packages it, labels it, repackages it and relabels it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Recalls
- Mar 18, 2020 · Class II · Aurobindo Pharma USA Inc.
CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed
Lots: Lot #: 105180004A, Exp. Date 03/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Phentermine: every company that makes it
- Form
- capsule
- Strength
- 15 mg
- Approval
- ANDA ANDA204318
- On the market since
- Mar 20, 2017
- Package NDCs
50090-3282-050090-3282-250090-3282-450090-3282-5- Official label
- DailyMed (National Library of Medicine), updated Aug 7, 2021
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