Tussin CF - 49580-0126-4 - (Robitussin CF)

Alphabetical Index


Drug Information of Tussin CF

Product NDC: 49580-0126
Proprietary Name: Tussin CF
Non Proprietary Name: Robitussin CF
Active Ingredient(s): 10; 100; 5    mg/5mL; mg/5mL; mg/5mL & nbsp;   Robitussin CF
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Tussin CF

Product NDC: 49580-0126
Labeler Name: Aaron Industries Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050110

Package Information of Tussin CF

Package NDC: 49580-0126-4
Package Description: 118 mL in 1 BOTTLE, PLASTIC (49580-0126-4)

NDC Information of Tussin CF

NDC Code 49580-0126-4
Proprietary Name Tussin CF
Package Description 118 mL in 1 BOTTLE, PLASTIC (49580-0126-4)
Product NDC 49580-0126
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Robitussin CF
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20050110
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Aaron Industries Inc
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 10; 100; 5
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Tussin CF


General Information