ALLI - 0135-0461-02 - (orlistat)

Alphabetical Index


Drug Information of ALLI

Product NDC: 0135-0461
Proprietary Name: ALLI
Non Proprietary Name: orlistat
Active Ingredient(s): 60    mg/1 & nbsp;   orlistat
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of ALLI

Product NDC: 0135-0461
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021887
Marketing Category: NDA
Start Marketing Date: 20070207

Package Information of ALLI

Package NDC: 0135-0461-02
Package Description: 90 CAPSULE in 1 BOTTLE (0135-0461-02)

NDC Information of ALLI

NDC Code 0135-0461-02
Proprietary Name ALLI
Package Description 90 CAPSULE in 1 BOTTLE (0135-0461-02)
Product NDC 0135-0461
Product Type Name HUMAN OTC DRUG
Non Proprietary Name orlistat
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070207
Marketing Category Name NDA
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name ORLISTAT
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ALLI


General Information