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Ritussin Expectorant - 53807-408-16 - (GUAIFENESIN)

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Drug Information of Ritussin Expectorant

Product NDC: 53807-408
Proprietary Name: Ritussin Expectorant
Non Proprietary Name: GUAIFENESIN
Active Ingredient(s): 100    mg/5mL & nbsp;   GUAIFENESIN
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Ritussin Expectorant

Product NDC: 53807-408
Labeler Name: Rij Pharmaceutical Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19990316

Package Information of Ritussin Expectorant

Package NDC: 53807-408-16
Package Description: 473 mL in 1 BOTTLE (53807-408-16)

NDC Information of Ritussin Expectorant

NDC Code 53807-408-16
Proprietary Name Ritussin Expectorant
Package Description 473 mL in 1 BOTTLE (53807-408-16)
Product NDC 53807-408
Product Type Name HUMAN OTC DRUG
Non Proprietary Name GUAIFENESIN
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19990316
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rij Pharmaceutical Corporation
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Ritussin Expectorant


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