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all day pain relief - 42254-230-14 - (Naproxen Sodium)

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Drug Information of all day pain relief

Product NDC: 42254-230
Proprietary Name: 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 all day pain relief

Product NDC: 42254-230
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 19970114

Package Information of all day pain relief

Package NDC: 42254-230-14
Package Description: 14 TABLET in 1 BOTTLE (42254-230-14)

NDC Information of all day pain relief

NDC Code 42254-230-14
Proprietary Name all day pain relief
Package Description 14 TABLET in 1 BOTTLE (42254-230-14)
Product NDC 42254-230
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 Rebel Distributors Corp
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of all day pain relief


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