Tramadol Hydrochloride

Product NDC

63739-671

11-digit product format

637390671

Labeler code

63739

Product ID

63739-671_6b8ee068-056b-4222-b593-abd179f8c4e9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tramadol Hydrochloride

Dosage form

TABLET, COATED

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA076003

Marketing category

ANDA

Marketing start

2010-11-15

Marketing end

0000-00-00

Substance

TRAMADOL HYDROCHLORIDE

Active strength

50 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