NDC 67544-700
Loperamide Hydrochloride 2 mg capsule
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from Mylan Pharmaceuticals Inc.'s NDC 0378-2100.
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 Mylan Pharmaceuticals Inc. names for other drugs.
Repackaging site
- Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN, United States · repackages it
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Loperamide: every company that makes it
- Form
- capsule
- Strength
- 2 mg
- Approval
- ANDA ANDA072741
- On the market since
- Oct 12, 2012
- Package NDCs
67544-700-5367544-700-60- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?