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pain relief - 0363-0140-82 - (Naproxen sodium)

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Drug Information of pain relief

Product NDC: 0363-0140
Proprietary Name: pain relief
Non Proprietary Name: Naproxen sodium
Active Ingredient(s): 220    mg/1 & nbsp;   Naproxen sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of pain relief

Product NDC: 0363-0140
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20111022

Package Information of pain relief

Package NDC: 0363-0140-82
Package Description: 200 TABLET, FILM COATED in 1 BOTTLE (0363-0140-82)

NDC Information of pain relief

NDC Code 0363-0140-82
Proprietary Name pain relief
Package Description 200 TABLET, FILM COATED in 1 BOTTLE (0363-0140-82)
Product NDC 0363-0140
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111022
Marketing Category Name ANDA
Labeler Name Walgreen Company
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of pain relief


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