Package 50804-176-68

Brand: goodsense ultra strength antacid peppermint

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 50804-176-68
Digits Only 5080417668
Product NDC 50804-176
Description

72 TABLET, CHEWABLE in 1 BOTTLE (50804-176-68)

Marketing

Marketing Status
Marketed Since 2018-08-08
Brand goodsense ultra strength antacid peppermint
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "089a34c1-69eb-43f8-ad0e-b37ea6bff7c0", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["04950b56-7760-4b6c-8110-86b6a3f795b4"], "manufacturer_name": ["GoodSense"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (50804-176-68)", "package_ndc": "50804-176-68", "marketing_start_date": "20180808"}], "brand_name": "GOODSENSE Ultra Strength Antacid Peppermint", "product_id": "50804-176_089a34c1-69eb-43f8-ad0e-b37ea6bff7c0", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "50804-176", "generic_name": "Calcium carbonate", "labeler_name": "GoodSense", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GOODSENSE Ultra Strength Antacid Peppermint", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180808", "listing_expiration_date": "20261231"}