NDC 71872-7242
Diphenhydramine Hydrochloride 25 mg per 10 mL solution
On the label: Medical Purchasing Solutions, LLC.. It's repackaged: Medical Purchasing Solutions, LLC. rebottles it from Pharmaceutical Associates, Inc.'s NDC 0121-0978.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma | Greenville, SC, United States | Makes it | No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action |
Repackaging site
- Medical Purchasing Solutions, LLC, Scottsdale, AZ, 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
- Diphenhydramine: every company that makes it
- Form
- solution, oral
- Strength
- 25 mg per 10 mL
- Approval
- ANDA ANDA087513
- On the market since
- Feb 10, 1982
- Package NDCs
71872-7242-1- Official label
- DailyMed (National Library of Medicine), updated Apr 27, 2023
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