Package 68998-103-72

Brand: marc glassman ultra strength

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 68998-103-72
Digits Only 6899810372
Product NDC 68998-103
Description

72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (68998-103-72)

Marketing

Marketing Status
Marketed Since 2019-04-17
Brand marc glassman ultra strength
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f263ceb-18cb-5b09-e063-6394a90a1890", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["35372a73-9578-4f46-9005-019fd8dd2e18"], "manufacturer_name": ["MARC GLASSMAN, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (68998-103-72)", "package_ndc": "68998-103-72", "marketing_start_date": "20190417"}], "brand_name": "Marc Glassman Ultra Strength", "product_id": "68998-103_3f263ceb-18cb-5b09-e063-6394a90a1890", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "68998-103", "generic_name": "Calcium Carbonate", "labeler_name": "MARC GLASSMAN, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Marc Glassman", "brand_name_suffix": "Ultra Strength", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190417", "listing_expiration_date": "20261231"}