NDC 58118-8020

Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate 2 mg / 8 mg tablet

On the label: Clinical Solutions Wholesale. It's repackaged: Clinical Solutions Wholesale rebottles it from SpecGx LLC's NDC 0406-8020.

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 SpecGx LLC names for other drugs.

Repackaging site

Product details

Generic drug
Buprenorphine and Naloxone: every company that makes it
Form
tablet, sublingual
Strength
2 mg / 8 mg
Approval
ANDA ANDA207000
On the market since
Dec 13, 2017
Package NDCs
58118-8020-8
Official label
DailyMed (National Library of Medicine), updated Jan 9, 2024

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