Orphenadrine Citrate

Product NDC

68788-9306

11-digit product format

687889306

Labeler code

68788

Product ID

68788-9306_ee08d037-4c16-4590-aaed-d7162687b8f1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Orphenadrine Citrate

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA040327

Marketing category

ANDA

Marketing start

2000-02-15

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record