Buprenorphine (Teva Pharmaceuticals USA, Inc.)


Welcome to the PulseAid listing for the Buprenorphine drug offered from Teva Pharmaceuticals USA, Inc.. This Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Teva Pharmaceuticals USA, Inc.
NON-PROPRIETARY NAME: Buprenorphine
SUBSTANCE NAME: BUPRENORPHINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA]
ROUTE: TRANSDERMAL
DOSAGE FORM: PATCH, EXTENDED RELEASE
MARKETING CATEGORY NAME: NDA AUTHORIZED GENERIC
START MARKETING DATE: 2017-05-30
END MARKETING DATE: 0000-00-00


Buprenorphine HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBuprenorphine from Teva Pharmaceuticals USA, Inc.
LABELER NAME: Teva Pharmaceuticals USA, Inc.
DEA SCHEDULE: CIII
ACTIVE STRENGTH: 5(ug/h)
START MARKETING DATE: 2017-05-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0093-3600_6f01f14e-5b47-4544-9656-d471cebe03ee
PRODUCT NDC: 0093-3600
APPLICATION NUMBER: NDA021306

Other BUPRENORPHINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Lake Erie Medical & Surgical Supply DBA Quality Care Products LLCButrans
Purdue Pharma LPButrans
Rhodes Pharmaceuticals L.P.Buprenorphine
Teva Pharmaceuticals USA, Inc.Buprenorphine