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Zubsolv

NDC 82111-203 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Generic namebuprenorphine hydrochloride and naloxone hydrochloride
Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryNew Drug Application (innovator) · App NDA204242
Dosage form / routeTABLET, ORALLY DISINTEGRATING · SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (2.9 mg/1)
NALOXONE HYDROCHLORIDE (.71 mg/1)
Marketing started20260612
Package count1

External sources

Source: openFDA. Public-domain (CC0).