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rx act all day pain relief - 37808-140-82 - (Naproxen sodium)

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Drug Information of rx act all day pain relief

Product NDC: 37808-140
Proprietary Name: rx act 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 rx act all day pain relief

Product NDC: 37808-140
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20080212

Package Information of rx act all day pain relief

Package NDC: 37808-140-82
Package Description: 200 TABLET, FILM COATED in 1 BOTTLE (37808-140-82)

NDC Information of rx act all day pain relief

NDC Code 37808-140-82
Proprietary Name rx act all day pain relief
Package Description 200 TABLET, FILM COATED in 1 BOTTLE (37808-140-82)
Product NDC 37808-140
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080212
Marketing Category Name ANDA
Labeler Name H E B
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of rx act all day pain relief


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