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naproxen sodium - 37808-608-27 - (Naproxen sodium)

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Drug Information of naproxen sodium

Product NDC: 37808-608
Proprietary Name: 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 naproxen sodium

Product NDC: 37808-608
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021920
Marketing Category: NDA
Start Marketing Date: 20110104

Package Information of naproxen sodium

Package NDC: 37808-608-27
Package Description: 1 BOTTLE in 1 CARTON (37808-608-27) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Information of naproxen sodium

NDC Code 37808-608-27
Proprietary Name naproxen sodium
Package Description 1 BOTTLE in 1 CARTON (37808-608-27) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product NDC 37808-608
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen sodium
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20110104
Marketing Category Name NDA
Labeler Name H E B
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of naproxen sodium


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