NDC 42858-353 – Buprenorphine

Buprenorphine 7.5 ug/h · Patch · Transdermal

Human Prescription Drug DEA schedule CIII

Product NDC42858-353

Product details

Brand name
Buprenorphine
Generic name
Buprenorphine
Labeler
Rhodes Pharmaceuticals LLC
Dosage form
Patch
Route
Transdermal
Marketing category
NDA AUTHORIZED GENERIC · NDA021306
Marketed since
July 3, 2017
Listing expires
December 31, 2027
Pharmacologic class
Partial Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Buprenorphine →

Package NDC codes (1)

Package NDCDescriptionSince
42858-353-404 POUCH in 1 CARTON (42858-353-40) / 1 PATCH in 1 POUCH / 168 h in 1 PATCHJul 5, 2017

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