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good sense all day pain relief - 0113-9490-71 - (Naproxen Sodium)

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Drug Information of good sense all day pain relief

Product NDC: 0113-9490
Proprietary Name: good sense all day pain relief
Non Proprietary Name: Naproxen Sodium
Active Ingredient(s): 220    mg/1 & nbsp;   Naproxen Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of good sense all day pain relief

Product NDC: 0113-9490
Labeler Name: L Perrigo Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 19970114

Package Information of good sense all day pain relief

Package NDC: 0113-9490-71
Package Description: 1 BOTTLE in 1 CARTON (0113-9490-71) > 50 TABLET in 1 BOTTLE

NDC Information of good sense all day pain relief

NDC Code 0113-9490-71
Proprietary Name good sense all day pain relief
Package Description 1 BOTTLE in 1 CARTON (0113-9490-71) > 50 TABLET in 1 BOTTLE
Product NDC 0113-9490
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970114
Marketing Category Name ANDA
Labeler Name L Perrigo Company
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of good sense all day pain relief


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