NDC 0093-3239 – Buprenorphine

Buprenorphine 7.5 ug/h · Patch, Extended Release · Transdermal

Human Prescription Drug DEA schedule CIII 1 recall

Product NDC0093-3239

Product details

Brand name
Buprenorphine
Generic name
Buprenorphine
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Patch, Extended Release
Route
Transdermal
Marketing category
ANDA · ANDA204937
Marketed since
December 27, 2021
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
0093-3239-404 POUCH in 1 CARTON (0093-3239-40) / 1 PATCH in 1 POUCH / 168 h in 1 PATCHDec 27, 2021

Recalls mentioning this NDC

Other Buprenorphine products