Naproxen - 76237-214-30 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 76237-214
Proprietary Name: Naproxen
Non Proprietary Name: Naproxen
Active Ingredient(s): 500    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 76237-214
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074201
Marketing Category: ANDA
Start Marketing Date: 20120125

Package Information of Naproxen

Package NDC: 76237-214-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-214-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Naproxen

NDC Code 76237-214-30
Proprietary Name Naproxen
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-214-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-214
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120125
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name NAPROXEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naproxen


General Information