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Trepoxen-250 - 68405-016-36 - (NAPROXEN,HISTIDINE)

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Drug Information of Trepoxen-250

Product NDC: 68405-016
Proprietary Name: Trepoxen-250
Non Proprietary Name: NAPROXEN,HISTIDINE
Active Ingredient(s):    & nbsp;   NAPROXEN,HISTIDINE
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Trepoxen-250

Product NDC: 68405-016
Labeler Name: Physician Therapeutics LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110203

Package Information of Trepoxen-250

Package NDC: 68405-016-36
Package Description: 1 KIT in 1 KIT (68405-016-36) * 30 TABLET in 1 BOTTLE (52959-190-30) * 90 CAPSULE in 1 BOTTLE

NDC Information of Trepoxen-250

NDC Code 68405-016-36
Proprietary Name Trepoxen-250
Package Description 1 KIT in 1 KIT (68405-016-36) * 30 TABLET in 1 BOTTLE (52959-190-30) * 90 CAPSULE in 1 BOTTLE
Product NDC 68405-016
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NAPROXEN,HISTIDINE
Dosage Form Name KIT
Route Name
Start Marketing Date 20110203
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Physician Therapeutics LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Trepoxen-250


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