Tramadol Hydrochloride

Product NDC

66267-563

11-digit product format

662670563

Labeler code

66267

Product ID

66267-563_9cadc4db-4181-004a-e053-2a95a90a2528

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tramadol Hydrochloride

Dosage form

TABLET, COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

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

2021-12-31

Current FDA listing

Historical FDA.report record