TRAMADOL HYDROCHLORIDE

Product NDC

50436-0824

11-digit product format

504360824

Labeler code

50436

Product ID

50436-0824_29205219-3034-435c-a04a-f65586ff75b3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

TRAMADOL HYDROCHLORIDE

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA091607

Marketing category

ANDA

Marketing start

2011-12-30

Marketing end

0000-00-00

Substance

TRAMADOL HYDROCHLORIDE

Active strength

200 mg/1

Pharmacologic classes

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

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record