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care one all day pain relief - 41520-368-71 - (Naproxen Sodium)

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Drug Information of care one all day pain relief

Product NDC: 41520-368
Proprietary Name: care one 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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of care one all day pain relief

Product NDC: 41520-368
Labeler Name: American Sales Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20040405

Package Information of care one all day pain relief

Package NDC: 41520-368-71
Package Description: 1 BOTTLE in 1 CARTON (41520-368-71) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of care one all day pain relief

NDC Code 41520-368-71
Proprietary Name care one all day pain relief
Package Description 1 BOTTLE in 1 CARTON (41520-368-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 41520-368
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040405
Marketing Category Name ANDA
Labeler Name American Sales Company
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of care one all day pain relief


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