NDC 42858-602

Buprenorphine and Naloxone 2 mg / 8 mg tablet

On the label: Rhodes Pharmaceuticals L.P..

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Halo Pharmaceutical IncWhippany, NJ, United StatesMakes it No problems foundDec 8, 2025 · 13 inspections
Knoa Pharmaceuticals LLCWilson, NC, United StatesMakes it Problems found, fixed voluntarilySep 26, 2025 · 9 inspections

Product details

Generic drug
Buprenorphine and Naloxone: every company that makes it
Form
tablet, sublingual
Strength
2 mg / 8 mg
Approval
ANDA ANDA205601
On the market since
Apr 13, 2020
Package NDCs
42858-602-03
Official label
DailyMed (National Library of Medicine), updated May 1, 2026

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