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Theraprofen-90 - 68405-088-36 - (IBUPROFEN, .GAMMA.-AMINOBUTYRIC ACID)

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Drug Information of Theraprofen-90

Product NDC: 68405-088
Proprietary Name: Theraprofen-90
Non Proprietary Name: IBUPROFEN, .GAMMA.-AMINOBUTYRIC ACID
Active Ingredient(s):    & nbsp;   IBUPROFEN, .GAMMA.-AMINOBUTYRIC ACID
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Theraprofen-90

Product NDC: 68405-088
Labeler Name: Physician Therapeutics LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110207

Package Information of Theraprofen-90

Package NDC: 68405-088-36
Package Description: 1 KIT in 1 KIT (68405-088-36) * 60 TABLET in 1 BOTTLE (52959-076-60) * 90 CAPSULE in 1 BOTTLE

NDC Information of Theraprofen-90

NDC Code 68405-088-36
Proprietary Name Theraprofen-90
Package Description 1 KIT in 1 KIT (68405-088-36) * 60 TABLET in 1 BOTTLE (52959-076-60) * 90 CAPSULE in 1 BOTTLE
Product NDC 68405-088
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name IBUPROFEN, .GAMMA.-AMINOBUTYRIC ACID
Dosage Form Name KIT
Route Name
Start Marketing Date 20110207
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Physician Therapeutics LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Theraprofen-90


General Information