Nalfon - 42195-600-10 - (fenoprofen calcium)

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Drug Information of Nalfon

Product NDC: 42195-600
Proprietary Name: Nalfon
Non Proprietary Name: fenoprofen calcium
Active Ingredient(s): 200    mg/1 & nbsp;   fenoprofen calcium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nalfon

Product NDC: 42195-600
Labeler Name: Xspire Pharma
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017604
Marketing Category: NDA
Start Marketing Date: 20120827

Package Information of Nalfon

Package NDC: 42195-600-10
Package Description: 100 CAPSULE in 1 BOTTLE (42195-600-10)

NDC Information of Nalfon

NDC Code 42195-600-10
Proprietary Name Nalfon
Package Description 100 CAPSULE in 1 BOTTLE (42195-600-10)
Product NDC 42195-600
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fenoprofen calcium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120827
Marketing Category Name NDA
Labeler Name Xspire Pharma
Substance Name FENOPROFEN CALCIUM
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 Nalfon


General Information