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Sunmark Antacid - 49348-019-39 - (Aluminum hydroxide, Magnesium hydroxide, Simethicone)

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Drug Information of Sunmark Antacid

Product NDC: 49348-019
Proprietary Name: Sunmark Antacid
Non Proprietary Name: Aluminum hydroxide, Magnesium hydroxide, Simethicone
Active Ingredient(s): 200; 20; 200    mg/5mL; mg/5mL; mg/5mL & nbsp;   Aluminum hydroxide, Magnesium hydroxide, Simethicone
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Sunmark Antacid

Product NDC: 49348-019
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part332
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20030913

Package Information of Sunmark Antacid

Package NDC: 49348-019-39
Package Description: 355 mL in 1 BOTTLE (49348-019-39)

NDC Information of Sunmark Antacid

NDC Code 49348-019-39
Proprietary Name Sunmark Antacid
Package Description 355 mL in 1 BOTTLE (49348-019-39)
Product NDC 49348-019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aluminum hydroxide, Magnesium hydroxide, Simethicone
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20030913
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE
Strength Number 200; 20; 200
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Sunmark Antacid


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