Orphenadrine Citrate

Product NDC

50436-7601

11-digit product format

504367601

Labeler code

50436

Product ID

50436-7601_258bd4ad-5886-4348-99dc-a496e07e309c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ORPHENADRINE CITRATE

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA040284

Marketing category

ANDA

Marketing start

1998-06-19

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record