Package 65197-300-11
Brand: gelusil
Generic: alumina, magnesia, simethiconePackage Facts
Identity
Package NDC
65197-300-11
Digits Only
6519730011
Product NDC
65197-300
Description
100 TABLET, CHEWABLE in 1 BOTTLE (65197-300-11)
Marketing
Marketing Status
Brand
gelusil
Generic
alumina, magnesia, simethicone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4406bf6b-b261-c6e1-e063-6294a90ae101", "openfda": {"upc": ["0365197300112"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S", "ETJ7Z6XBU4"], "rxcui": ["211633", "307747"], "spl_set_id": ["92fbeec1-1562-40f3-9734-41f133d494f9"], "manufacturer_name": ["WellSpring Pharmaceutical Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65197-300-10) / 10 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "65197-300-10", "marketing_start_date": "20080924"}, {"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (65197-300-11)", "package_ndc": "65197-300-11", "marketing_start_date": "20181201"}], "brand_name": "Gelusil", "product_id": "65197-300_4406bf6b-b261-c6e1-e063-6294a90ae101", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Skin Barrier Activity [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "65197-300", "generic_name": "Alumina, Magnesia, Simethicone", "labeler_name": "WellSpring Pharmaceutical Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Gelusil", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "200 mg/1"}, {"name": "DIMETHICONE, UNSPECIFIED", "strength": "24 mg/1"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "200 mg/1"}, {"name": "SILICON DIOXIDE", "strength": "1 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20080924", "listing_expiration_date": "20261231"}