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ORPHENADRINE CITRATE - 16590-177-71 - (ORPHENADRINE CITRATE)

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Drug Information of ORPHENADRINE CITRATE

Product NDC: 16590-177
Proprietary Name: ORPHENADRINE CITRATE
Non Proprietary Name: ORPHENADRINE CITRATE
Active Ingredient(s): 100    mg/1 & nbsp;   ORPHENADRINE CITRATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of ORPHENADRINE CITRATE

Product NDC: 16590-177
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040368
Marketing Category: ANDA
Start Marketing Date: 20000623

Package Information of ORPHENADRINE CITRATE

Package NDC: 16590-177-71
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16590-177-71)

NDC Information of ORPHENADRINE CITRATE

NDC Code 16590-177-71
Proprietary Name ORPHENADRINE CITRATE
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16590-177-71)
Product NDC 16590-177
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ORPHENADRINE CITRATE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20000623
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name ORPHENADRINE CITRATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of ORPHENADRINE CITRATE


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