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Equaline Naproxen Sodium - 41163-742-71 - (Naproxen sodium)

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Drug Information of Equaline Naproxen Sodium

Product NDC: 41163-742
Proprietary Name: Equaline Naproxen Sodium
Non Proprietary Name: Naproxen sodium
Active Ingredient(s): 220    mg/1 & nbsp;   Naproxen sodium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Equaline Naproxen Sodium

Product NDC: 41163-742
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021920
Marketing Category: NDA
Start Marketing Date: 20101123

Package Information of Equaline Naproxen Sodium

Package NDC: 41163-742-71
Package Description: 1 BOTTLE in 1 CARTON (41163-742-71) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Information of Equaline Naproxen Sodium

NDC Code 41163-742-71
Proprietary Name Equaline Naproxen Sodium
Package Description 1 BOTTLE in 1 CARTON (41163-742-71) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product NDC 41163-742
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen sodium
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20101123
Marketing Category Name NDA
Labeler Name Supervalu Inc
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Equaline Naproxen Sodium


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