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mucus relief - 11822-0498-1 - (Guaifenesin)

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Drug Information of mucus relief

Product NDC: 11822-0498
Proprietary Name: mucus relief
Non Proprietary Name: Guaifenesin
Active Ingredient(s): 600    mg/1 & nbsp;   Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of mucus relief

Product NDC: 11822-0498
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078912
Marketing Category: ANDA
Start Marketing Date: 20130320

Package Information of mucus relief

Package NDC: 11822-0498-1
Package Description: 1 BOTTLE in 1 CARTON (11822-0498-1) > 20 TABLET, EXTENDED RELEASE in 1 BOTTLE

NDC Information of mucus relief

NDC Code 11822-0498-1
Proprietary Name mucus relief
Package Description 1 BOTTLE in 1 CARTON (11822-0498-1) > 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product NDC 11822-0498
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130320
Marketing Category Name ANDA
Labeler Name Rite Aid Corporation
Substance Name GUAIFENESIN
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of mucus relief


General Information