CITRUCEL - 0135-0199-02 - (methylcellulose)

Alphabetical Index


Drug Information of CITRUCEL

Product NDC: 0135-0199
Proprietary Name: CITRUCEL
Non Proprietary Name: methylcellulose
Active Ingredient(s): 500    mg/1 & nbsp;   methylcellulose
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CITRUCEL

Product NDC: 0135-0199
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100201

Package Information of CITRUCEL

Package NDC: 0135-0199-02
Package Description: 100 TABLET in 1 BOTTLE (0135-0199-02)

NDC Information of CITRUCEL

NDC Code 0135-0199-02
Proprietary Name CITRUCEL
Package Description 100 TABLET in 1 BOTTLE (0135-0199-02)
Product NDC 0135-0199
Product Type Name HUMAN OTC DRUG
Non Proprietary Name methylcellulose
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name METHYLCELLULOSE (4000 MPA.S)
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of CITRUCEL


General Information