Buprenorphine

Product NDC

0093-3600

11-digit product format

000933600

Labeler code

0093

Product ID

0093-3600_aa750280-23ed-4d6d-9666-780dab437aab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Buprenorphine

Dosage form

PATCH, EXTENDED RELEASE

Route

TRANSDERMAL

Labeler

Teva Pharmaceuticals USA,

Application

NDA021306

Marketing category

NDA AUTHORIZED

Marketing start

2017-05-30

Marketing end

2019-03-31

Substance

BUPRENORPHINE

Active strength

5 ug/h

Pharmacologic classes

Partial Opioid

DEA schedule

CIII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record