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Guaifenesin - 50383-063-18 - (Guaifenesin)

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Drug Information of Guaifenesin

Product NDC: 50383-063
Proprietary Name: Guaifenesin
Non Proprietary Name: Guaifenesin
Active Ingredient(s): 100    mg/5mL & nbsp;   Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Guaifenesin

Product NDC: 50383-063
Labeler Name: Hi-Tech Pharmacal Co., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120307

Package Information of Guaifenesin

Package NDC: 50383-063-18
Package Description: 10 TRAY in 1 CASE (50383-063-18) > 10 CUP, UNIT-DOSE in 1 TRAY > 15 mL in 1 CUP, UNIT-DOSE

NDC Information of Guaifenesin

NDC Code 50383-063-18
Proprietary Name Guaifenesin
Package Description 10 TRAY in 1 CASE (50383-063-18) > 10 CUP, UNIT-DOSE in 1 TRAY > 15 mL in 1 CUP, UNIT-DOSE
Product NDC 50383-063
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20120307
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Hi-Tech Pharmacal Co., Inc.
Substance Name GUAIFENESIN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Guaifenesin


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