Tramadol Hydrochloride

Product NDC

50436-0821

11-digit product format

504360821

Labeler code

50436

Product ID

50436-0821_b30450ac-db81-4f63-9b85-cd0078cc31af

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tramadol Hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Unit Dose Services

Application

NDA022370

Marketing category

NDA

Marketing start

2015-07-01

Marketing end

0000-00-00

Substance

TRAMADOL HYDROCHLORIDE

Active strength

150 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