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all day relief - 49999-068-90 - (Naproxen Sodium)

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Drug Information of all day relief

Product NDC: 49999-068
Proprietary Name: all day 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 relief

Product NDC: 49999-068
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 19970109

Package Information of all day relief

Package NDC: 49999-068-90
Package Description: 90 TABLET in 1 BOTTLE (49999-068-90)

NDC Information of all day relief

NDC Code 49999-068-90
Proprietary Name all day relief
Package Description 90 TABLET in 1 BOTTLE (49999-068-90)
Product NDC 49999-068
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970109
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of all day relief


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