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Tramadol Hydrochloride - 68387-900-20 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 68387-900
Proprietary Name: Tramadol Hydrochloride
Non Proprietary Name: Tramadol Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Tramadol Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tramadol Hydrochloride

Product NDC: 68387-900
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076003
Marketing Category: ANDA
Start Marketing Date: 20090630

Package Information of Tramadol Hydrochloride

Package NDC: 68387-900-20
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (68387-900-20)

NDC Information of Tramadol Hydrochloride

NDC Code 68387-900-20
Proprietary Name Tramadol Hydrochloride
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (68387-900-20)
Product NDC 68387-900
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090630
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals Inc.
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Tramadol Hydrochloride


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