CARBATUSS - 58809-536-02 - (Carbetapentane Citrate, Phenylephrine Hydrochloride, Guaifenesin)

Alphabetical Index


Drug Information of CARBATUSS

Product NDC: 58809-536
Proprietary Name: CARBATUSS
Non Proprietary Name: Carbetapentane Citrate, Phenylephrine Hydrochloride, Guaifenesin
Active Ingredient(s): 20; 100; 10    mg/5mL; mg/5mL; mg/5mL & nbsp;   Carbetapentane Citrate, Phenylephrine Hydrochloride, Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of CARBATUSS

Product NDC: 58809-536
Labeler Name: GM Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20001101

Package Information of CARBATUSS

Package NDC: 58809-536-02
Package Description: 15 mL in 1 BOTTLE (58809-536-02)

NDC Information of CARBATUSS

NDC Code 58809-536-02
Proprietary Name CARBATUSS
Package Description 15 mL in 1 BOTTLE (58809-536-02)
Product NDC 58809-536
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbetapentane Citrate, Phenylephrine Hydrochloride, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20001101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name GM Pharmaceuticals, Inc.
Substance Name CARBETAPENTANE CITRATE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 20; 100; 10
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of CARBATUSS


General Information