Buprenorphine

Product NDC

50090-2924

11-digit product format

500902924

Labeler code

50090

Product ID

50090-2924_380e7f04-549c-47d7-842c-22836b2dfe12

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Buprenorphine Hydrochloride

Dosage form

TABLET

Route

SUBLINGUAL

Labeler

A-S Medication Solutions

Application

ANDA090819

Marketing category

ANDA

Marketing start

2015-04-10

Marketing end

0000-00-00

Substance

BUPRENORPHINE HYDROCHLORIDE

Active strength

8 mg/1

Pharmacologic classes

Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC]

DEA schedule

CIII

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record