Package 80513-611-02
Brand: sodium bicarbonate 10 gr (650 mg)
Generic: sodium bicarbonatePackage Facts
Identity
Package NDC
80513-611-02
Digits Only
8051361102
Product NDC
80513-611
Description
200 TABLET in 1 BOTTLE (80513-611-02)
Marketing
Marketing Status
Brand
sodium bicarbonate 10 gr (650 mg)
Generic
sodium bicarbonate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d912fde-5c7a-e74c-e063-6394a90a6e1f", "openfda": {"upc": ["0380513001849"], "unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["634e8d52-6d04-42f9-98f6-2634473b5dfd"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (80513-611-02)", "package_ndc": "80513-611-02", "marketing_start_date": "20250901"}], "brand_name": "Sodium Bicarbonate 10 GR (650 MG)", "product_id": "80513-611_3d912fde-5c7a-e74c-e063-6394a90a6e1f", "dosage_form": "TABLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "80513-611", "generic_name": "Sodium Bicarbonate", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Bicarbonate", "brand_name_suffix": "10 GR (650 MG)", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "650 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250901", "listing_expiration_date": "20261231"}