Orphenadrine Citrate

Product NDC

68084-820

11-digit product format

680840820

Labeler code

68084

Product ID

68084-820_999718ed-cd7d-7fbe-e053-2a95a90a7132

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ORPHENADRINE CITRATE

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

American Health Packaging

Application

ANDA040368

Marketing category

ANDA

Marketing start

2014-09-09

Marketing end

2020-10-31

Substance

ORPHENADRINE CITRATE

Active strength

100 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record