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Orphenadrine Citrate - 35356-987-60 - (Orphenadrine Citrate)

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Drug Information of Orphenadrine Citrate

Product NDC: 35356-987
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
Coding System: National Drug Codes(NDC)

Labeler Information of Orphenadrine Citrate

Product NDC: 35356-987
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040327
Marketing Category: ANDA
Start Marketing Date: 20000215

Package Information of Orphenadrine Citrate

Package NDC: 35356-987-60
Package Description: 60 TABLET in 1 BOTTLE (35356-987-60)

NDC Information of Orphenadrine Citrate

NDC Code 35356-987-60
Proprietary Name Orphenadrine Citrate
Package Description 60 TABLET in 1 BOTTLE (35356-987-60)
Product NDC 35356-987
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Orphenadrine Citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000215
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products 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


General Information