Tramadol Hydrochloride

Product NDC

35356-659

11-digit product format

353560659

Labeler code

35356

Product ID

35356-659_1c1ab81f-0f11-4d10-8986-4e1a1b779bd9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tramadol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076003

Marketing category

ANDA

Marketing start

2009-11-23

Marketing end

0000-00-00

Substance

TRAMADOL HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record