DECONEX - 50991-582-60 - (Guaifenesin, Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of DECONEX

Product NDC: 50991-582
Proprietary Name: DECONEX
Non Proprietary Name: Guaifenesin, Phenylephrine Hydrochloride
Active Ingredient(s): 390; 10    mg/1; mg/1 & nbsp;   Guaifenesin, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of DECONEX

Product NDC: 50991-582
Labeler Name: Poly Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120207

Package Information of DECONEX

Package NDC: 50991-582-60
Package Description: 60 CAPSULE in 1 BOTTLE (50991-582-60)

NDC Information of DECONEX

NDC Code 50991-582-60
Proprietary Name DECONEX
Package Description 60 CAPSULE in 1 BOTTLE (50991-582-60)
Product NDC 50991-582
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin, Phenylephrine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120207
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Poly Pharmaceuticals
Substance Name GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 390; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of DECONEX


General Information