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TOLMETIN SODIUM - 16590-987-90 - (TOLMETIN SODIUM)

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Drug Information of TOLMETIN SODIUM

Product NDC: 16590-987
Proprietary Name: TOLMETIN SODIUM
Non Proprietary Name: TOLMETIN SODIUM
Active Ingredient(s): 600    mg/1 & nbsp;   TOLMETIN SODIUM
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of TOLMETIN SODIUM

Product NDC: 16590-987
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074473
Marketing Category: ANDA
Start Marketing Date: 20091102

Package Information of TOLMETIN SODIUM

Package NDC: 16590-987-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (16590-987-90)

NDC Information of TOLMETIN SODIUM

NDC Code 16590-987-90
Proprietary Name TOLMETIN SODIUM
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (16590-987-90)
Product NDC 16590-987
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TOLMETIN SODIUM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091102
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name TOLMETIN SODIUM
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of TOLMETIN SODIUM


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