Package 69367-258-10

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 69367-258-10
Digits Only 6936725810
Product NDC 69367-258
Product ID 69367-258_43b42880-bab8-4580-8a00-ae13855d44a3
Description

1000 TABLET in 1 BOTTLE (69367-258-10)

Marketing

Marketing Status
Marketed Since 2022-10-10
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Sodium Bicarbonate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43b42880-bab8-4580-8a00-ae13855d44a3", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["9dcfc778-5fd6-4c68-8d37-a5385e374617"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (69367-258-10)", "package_ndc": "69367-258-10", "marketing_start_date": "20221010"}], "brand_name": "Sodium Bicarbonate", "product_id": "69367-258_43b42880-bab8-4580-8a00-ae13855d44a3", "dosage_form": "TABLET", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "69367-258", "generic_name": "Sodium Bicarbonate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "650 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221010", "listing_expiration_date": "20261231"}