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TOLMETIN SODIUM - 53489-506-90 - (tolmetin sodium)

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Drug Information of TOLMETIN SODIUM

Product NDC: 53489-506
Proprietary Name: TOLMETIN SODIUM
Non Proprietary Name: tolmetin sodium
Active Ingredient(s): 200    mg/1 & nbsp;   tolmetin sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of TOLMETIN SODIUM

Product NDC: 53489-506
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073311
Marketing Category: ANDA
Start Marketing Date: 20090904

Package Information of TOLMETIN SODIUM

Package NDC: 53489-506-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (53489-506-90)

NDC Information of TOLMETIN SODIUM

NDC Code 53489-506-90
Proprietary Name TOLMETIN SODIUM
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (53489-506-90)
Product NDC 53489-506
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tolmetin sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090904
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name TOLMETIN SODIUM
Strength Number 200
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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