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Naproxen Sodium - 55111-272-24 - (Naproxen Sodium)

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Drug Information of Naproxen Sodium

Product NDC: 55111-272
Proprietary Name: Naproxen Sodium
Non Proprietary Name: Naproxen Sodium
Active Ingredient(s): 220    mg/1 & nbsp;   Naproxen Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen Sodium

Product NDC: 55111-272
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075168
Marketing Category: ANDA
Start Marketing Date: 19980729

Package Information of Naproxen Sodium

Package NDC: 55111-272-24
Package Description: 1 BOTTLE in 1 CARTON (55111-272-24) > 24 TABLET, COATED in 1 BOTTLE

NDC Information of Naproxen Sodium

NDC Code 55111-272-24
Proprietary Name Naproxen Sodium
Package Description 1 BOTTLE in 1 CARTON (55111-272-24) > 24 TABLET, COATED in 1 BOTTLE
Product NDC 55111-272
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19980729
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Naproxen Sodium


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