Package 69790-820-33

Brand: uline antacid

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 69790-820-33
Digits Only 6979082033
Product NDC 69790-820
Description

50 PACKET in 1 BOX (69790-820-33) / 2 TABLET, CHEWABLE in 1 PACKET

Marketing

Marketing Status
Marketed Since 2019-10-07
Brand uline antacid
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e4c0f0f-30c8-6e2b-e063-6294a90accbc", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["313884"], "spl_set_id": ["9014f295-e816-9bcd-e053-2a95a90ae103"], "manufacturer_name": ["Uline"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (69790-820-33)  / 2 TABLET, CHEWABLE in 1 PACKET", "package_ndc": "69790-820-33", "marketing_start_date": "20191007"}], "brand_name": "Uline Antacid", "product_id": "69790-820_3e4c0f0f-30c8-6e2b-e063-6294a90accbc", "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": "69790-820", "generic_name": "calcium carbonate", "labeler_name": "Uline", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Uline Antacid", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "420 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191007", "listing_expiration_date": "20261231"}