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pain relief - 21130-140-82 - (Naproxen sodium)

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Drug Information of pain relief

Product NDC: 21130-140
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: 21130-140
Labeler Name: Safeway
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20081003

Package Information of pain relief

Package NDC: 21130-140-82
Package Description: 200 TABLET, FILM COATED in 1 BOTTLE (21130-140-82)

NDC Information of pain relief

NDC Code 21130-140-82
Proprietary Name pain relief
Package Description 200 TABLET, FILM COATED in 1 BOTTLE (21130-140-82)
Product NDC 21130-140
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081003
Marketing Category Name ANDA
Labeler Name Safeway
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of pain relief


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