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Naproxen Tablets - 55111-366-05 - (Naproxen Tablets)

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Drug Information of Naproxen Tablets

Product NDC: 55111-366
Proprietary Name: Naproxen Tablets
Non Proprietary Name: Naproxen Tablets
Active Ingredient(s): 250    mg/1 & nbsp;   Naproxen Tablets
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen Tablets

Product NDC: 55111-366
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075927
Marketing Category: ANDA
Start Marketing Date: 20040605

Package Information of Naproxen Tablets

Package NDC: 55111-366-05
Package Description: 500 TABLET in 1 BOTTLE (55111-366-05)

NDC Information of Naproxen Tablets

NDC Code 55111-366-05
Proprietary Name Naproxen Tablets
Package Description 500 TABLET in 1 BOTTLE (55111-366-05)
Product NDC 55111-366
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen Tablets
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040605
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name NAPROXEN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naproxen Tablets


General Information