NDC 71872-7170

Procainamide Hydrochloride 1000 mg injection

On the label: Medical Purchasing Solutions, LLC.. It's repackaged: Medical Purchasing Solutions, LLC. rebottles it from Nexus Pharamaceuticals Inc.'s NDC 14789-900.

Where the pills inside were made

This label doesn't name the factory that makes the drug (it lists 1 site that tests it). 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 Nexus Pharamaceuticals Inc. names for other drugs.

Repackaging site

Product details

Generic drug
Procainamide: every company that makes it
Form
injection
Strength
1000 mg
Approval
ANDA ANDA206332
On the market since
Oct 18, 2017
Package NDCs
71872-7170-1
Official label
DailyMed (National Library of Medicine), updated Jul 31, 2019

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?