Divista - 52747-110-60 - (Chromium Picolinate)

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Drug Information of Divista

Product NDC: 52747-110
Proprietary Name: Divista
Non Proprietary Name: Chromium Picolinate
Active Ingredient(s): 2; 1000; 15; 1; 300; 25    mg/1; ug/1; ug/1; mg/1; mg/1; mg/1 & nbsp;   Chromium Picolinate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Divista

Product NDC: 52747-110
Labeler Name: US Pharmaceutical Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100710

Package Information of Divista

Package NDC: 52747-110-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC (52747-110-60)

NDC Information of Divista

NDC Code 52747-110-60
Proprietary Name Divista
Package Description 60 CAPSULE in 1 BOTTLE, PLASTIC (52747-110-60)
Product NDC 52747-110
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chromium Picolinate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100710
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name US Pharmaceutical Corporation
Substance Name BIOTIN; CHROMIUM PICOLINATE; CYANOCOBALAMIN; FOLIC ACID; OMEGA-3-ACID ETHYL ESTERS; PYRIDOXINE
Strength Number 2; 1000; 15; 1; 300; 25
Strength Unit mg/1; ug/1; ug/1; mg/1; mg/1; mg/1
Pharmaceutical Classes Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]

Complete Information of Divista


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