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POLY-TUSSIN - 50991-529-15 - (Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin)

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Drug Information of POLY-TUSSIN

Product NDC: 50991-529
Proprietary Name: POLY-TUSSIN
Non Proprietary Name: Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin
Active Ingredient(s): 7.5; 50; 5    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of POLY-TUSSIN

Product NDC: 50991-529
Labeler Name: Poly Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20091116

Package Information of POLY-TUSSIN

Package NDC: 50991-529-15
Package Description: 15 mL in 1 BOTTLE (50991-529-15)

NDC Information of POLY-TUSSIN

NDC Code 50991-529-15
Proprietary Name POLY-TUSSIN
Package Description 15 mL in 1 BOTTLE (50991-529-15)
Product NDC 50991-529
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20091116
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Poly Pharmaceuticals, Inc.
Substance Name DIHYDROCODEINE BITARTRATE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 7.5; 50; 5
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of POLY-TUSSIN


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