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up and up naproxen sodium - 11673-368-82 - (Naproxen Sodium)

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Drug Information of up and up naproxen sodium

Product NDC: 11673-368
Proprietary Name: up and up naproxen sodium
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 up and up naproxen sodium

Product NDC: 11673-368
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20090624

Package Information of up and up naproxen sodium

Package NDC: 11673-368-82
Package Description: 1 BOTTLE in 1 CARTON (11673-368-82) > 200 TABLET, FILM COATED in 1 BOTTLE

NDC Information of up and up naproxen sodium

NDC Code 11673-368-82
Proprietary Name up and up naproxen sodium
Package Description 1 BOTTLE in 1 CARTON (11673-368-82) > 200 TABLET, FILM COATED in 1 BOTTLE
Product NDC 11673-368
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090624
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of up and up naproxen sodium


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