NDC Code(s) : 32909-717-01
Packager : E-Z-EM Canada Inc

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

E-Z-Cat DryBarium Sulfate POWDER, FOR SUSPENSION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:32909-717
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Barium Sulfate(UNII: 25BB7EKE2E)
(Barium Sulfate - UNII:25BB7EKE2E) 		Barium Sulfate400 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
anhydrous citric acid(UNII: XF417D3PSL)
carboxymethylcellulose sodium, unspecified form(UNII: K679OBS311)
carrageenan sodium(UNII: 7CY8BVL34N)
dimethicone 1000(UNII: MCU2324216)
ethyl vanillin(UNII: YC9ST449YJ)
polysorbate 80(UNII: 6OZP39ZG8H)
saccharin sodium(UNII: SB8ZUX40TY)
silicon dioxide(UNII: ETJ7Z6XBU4)
sorbitol(UNII: 506T60A25R)
trisodium citrate dihydrate(UNII: B22547B95K)
xanthan gum(UNII: TTV12P4NEE)
Product Characteristics
Color WHITE Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:32909-717-0112 in 1 CARTON 28/09/2017
150 in 1 BOX
123 g in 1 POUCH Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA208036 09/28/2017

PRINCIPAL DISPLAY PANEL

E-Z-CAT DRY Box
NDC: 32909-717-01

e-z-cat-dry-box

E-Z-CAT DRY Box Labels

e-z-cat-dry-boxe-z-cat-dry-box