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Tramadol Hydrochloride - 52125-377-02 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 52125-377
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tramadol Hydrochloride

Product NDC: 52125-377
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076003
Marketing Category: ANDA
Start Marketing Date: 20130513

Package Information of Tramadol Hydrochloride

Package NDC: 52125-377-02
Package Description: 30 TABLET, COATED in 1 VIAL (52125-377-02)

NDC Information of Tramadol Hydrochloride

NDC Code 52125-377-02
Proprietary Name Tramadol Hydrochloride
Package Description 30 TABLET, COATED in 1 VIAL (52125-377-02)
Product NDC 52125-377
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20130513
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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