Drugplain

KO-LANTA 200 mg/5mL

aluminum hydroxide, magnesium hydroxide, dimethicone · SUSPENSION · Geri-Care Pharmaceuticals, Corp

No Recall History
Plain English

KO-LANTA is a suspension containing aluminum hydroxide, magnesium hydroxide, dimethicone at 200 mg/5mL, taken oral. Manufactured by Geri-Care Pharmaceuticals, Corp.

Key Facts

Brand Name
KO-LANTA
Generic Name
aluminum hydroxide, magnesium hydroxide, dimethicone
NDC Code (Product)
57896-004
Manufacturer
Geri-Care Pharmaceuticals, Corp
Strength
200 mg/5mL
Dosage Form
SUSPENSION
Route
ORAL
Marketing Status
Application #
M001
Marketing Start
01/01/2020

Recall History

No Recall History

Frequently Asked Questions

What is KO-LANTA used for?

KO-LANTA contains aluminum hydroxide, magnesium hydroxide, dimethicone. It is a suspension taken oral. Consult your doctor for specific uses.

Is KO-LANTA a controlled substance?

KO-LANTA is not classified as a controlled substance by the DEA.

What is the generic name for KO-LANTA?

The generic name for KO-LANTA is aluminum hydroxide, magnesium hydroxide, dimethicone. There are 12 other brand versions of aluminum hydroxide, magnesium hydroxide, dimethicone.

What is the NDC code for KO-LANTA 200 mg/5mL?

The NDC (National Drug Code) for KO-LANTA 200 mg/5mL is 57896-004, listed by Geri-Care Pharmaceuticals, Corp.