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Tramadol Hydrochloride - 63629-4899-7 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 63629-4899
Proprietary Name: Tramadol Hydrochloride
Non Proprietary Name: Tramadol Hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   Tramadol Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Tramadol Hydrochloride

Product NDC: 63629-4899
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022370
Marketing Category: NDA
Start Marketing Date: 20120314

Package Information of Tramadol Hydrochloride

Package NDC: 63629-4899-7
Package Description: 40 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-4899-7)

NDC Information of Tramadol Hydrochloride

NDC Code 63629-4899-7
Proprietary Name Tramadol Hydrochloride
Package Description 40 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-4899-7)
Product NDC 63629-4899
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120314
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Tramadol Hydrochloride


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