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Tramadol Hydrochloride and Acetaminophen - 68387-497-30 - (tramadol hydrochloride and acetaminophen)

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Drug Information of Tramadol Hydrochloride and Acetaminophen

Product NDC: 68387-497
Proprietary Name: Tramadol Hydrochloride and Acetaminophen
Non Proprietary Name: tramadol hydrochloride and acetaminophen
Active Ingredient(s): 325; 37.5    mg/1; mg/1 & nbsp;   tramadol hydrochloride and acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tramadol Hydrochloride and Acetaminophen

Product NDC: 68387-497
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076475
Marketing Category: ANDA
Start Marketing Date: 20091019

Package Information of Tramadol Hydrochloride and Acetaminophen

Package NDC: 68387-497-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (68387-497-30)

NDC Information of Tramadol Hydrochloride and Acetaminophen

NDC Code 68387-497-30
Proprietary Name Tramadol Hydrochloride and Acetaminophen
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (68387-497-30)
Product NDC 68387-497
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091019
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals Inc.
Substance Name ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Strength Number 325; 37.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Tramadol Hydrochloride and Acetaminophen


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