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GILTUSS TOTAL RELEASE - 58552-317-02 - (Guaifenesin, Dextromethorphan HBr, and Phenylephrine HCl)

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Drug Information of GILTUSS TOTAL RELEASE

Product NDC: 58552-317
Proprietary Name: GILTUSS TOTAL RELEASE
Non Proprietary Name: Guaifenesin, Dextromethorphan HBr, and Phenylephrine HCl
Active Ingredient(s): 28; 388; 10    mg/1; mg/1; mg/1 & nbsp;   Guaifenesin, Dextromethorphan HBr, and Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of GILTUSS TOTAL RELEASE

Product NDC: 58552-317
Labeler Name: Gil Pharmaceutical Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20091019

Package Information of GILTUSS TOTAL RELEASE

Package NDC: 58552-317-02
Package Description: 12 BLISTER PACK in 1 CARTON (58552-317-02) > 2 TABLET in 1 BLISTER PACK

NDC Information of GILTUSS TOTAL RELEASE

NDC Code 58552-317-02
Proprietary Name GILTUSS TOTAL RELEASE
Package Description 12 BLISTER PACK in 1 CARTON (58552-317-02) > 2 TABLET in 1 BLISTER PACK
Product NDC 58552-317
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin, Dextromethorphan HBr, and Phenylephrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091019
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Gil Pharmaceutical Corp
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 28; 388; 10
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of GILTUSS TOTAL RELEASE


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