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Atuss DS Tannate Suspension - 59702-800-15 - (Tannate Suspension)

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Drug Information of Atuss DS Tannate Suspension

Product NDC: 59702-800
Proprietary Name: Atuss DS Tannate Suspension
Non Proprietary Name: Tannate Suspension
Active Ingredient(s): 4; 30; 30    mg/5mL; mg/5mL; mg/5mL & nbsp;   Tannate Suspension
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Atuss DS Tannate Suspension

Product NDC: 59702-800
Labeler Name: Atley Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20061121

Package Information of Atuss DS Tannate Suspension

Package NDC: 59702-800-15
Package Description: 15 mL in 1 BOTTLE (59702-800-15)

NDC Information of Atuss DS Tannate Suspension

NDC Code 59702-800-15
Proprietary Name Atuss DS Tannate Suspension
Package Description 15 mL in 1 BOTTLE (59702-800-15)
Product NDC 59702-800
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tannate Suspension
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20061121
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Atley Pharmaceuticals, Inc.
Substance Name CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 4; 30; 30
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],Sigma-1 Agonist [EPC],Uncompetitive NMDA Receptor Antagonists [MoA],Sigma-1 Receptor Agonists [MoA],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Atuss DS Tannate Suspension


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