Naproxen - 68788-9906-1 - (Naproxen)

Alphabetical Index


Drug Information of Naproxen

Product NDC: 68788-9906
Proprietary Name: Naproxen
Non Proprietary Name: Naproxen
Active Ingredient(s): 375    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 68788-9906
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075927
Marketing Category: ANDA
Start Marketing Date: 20120130

Package Information of Naproxen

Package NDC: 68788-9906-1
Package Description: 100 TABLET in 1 BOTTLE (68788-9906-1)

NDC Information of Naproxen

NDC Code 68788-9906-1
Proprietary Name Naproxen
Package Description 100 TABLET in 1 BOTTLE (68788-9906-1)
Product NDC 68788-9906
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120130
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name NAPROXEN
Strength Number 375
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