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Varibar Thin Liquid

These highlights do not include all the information needed to useVARIBAR THIN LIQUID safely and effectively. Initial U.S. Approval: 2016

Approved
Approval ID

59493c83-3941-cc84-cc37-a8696ae42873

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 20, 2023

Manufacturers
FDA

E-Z-EM Canada Inc

DUNS: 204211163

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

barium sulfate

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code32909-105
Application NumberNDA208036
Product Classification
M
Marketing Category
C73594
G
Generic Name
barium sulfate
Product Specifications
Route of AdministrationORAL
Effective DateApril 30, 2019
FDA Product Classification

INGREDIENTS (11)

Barium SulfateActive
Quantity: .81 g in 1 g
Code: 25BB7EKE2E
Classification: ACTIB
anhydrous citric acidInactive
Code: XF417D3PSL
Classification: IACT
carboxymethylcellulose sodiumInactive
Code: K679OBS311
Classification: IACT
dimethicone 1000Inactive
Code: MCU2324216
Classification: IACT
polysorbate 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
maltodextrinInactive
Code: 7CVR7L4A2D
Classification: IACT
silicon dioxideInactive
Code: ETJ7Z6XBU4
Classification: IACT
sorbitolInactive
Code: 506T60A25R
Classification: IACT
trisodium citrate dihydrateInactive
Code: B22547B95K
Classification: IACT
xylitolInactive
Code: VCQ006KQ1E
Classification: IACT
saccharin sodiumInactive
Code: SB8ZUX40TY
Classification: IACT

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Varibar Thin Liquid - FDA Drug Approval Details