Package 54738-020-03

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 54738-020-03
Digits Only 5473802003
Product NDC 54738-020
Description

1000 TABLET in 1 BOTTLE, PLASTIC (54738-020-03)

Marketing

Marketing Status
Marketed Since 2015-05-01
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5cc6cec2-9f03-6cf9-e053-2991aa0ada77", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["fa10d93d-b3ed-4675-a117-f573d9e72bca"], "manufacturer_name": ["Richmond Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (54738-020-03)", "package_ndc": "54738-020-03", "marketing_start_date": "20150501"}], "brand_name": "SODIUM BICARBONATE", "product_id": "54738-020_5cc6cec2-9f03-6cf9-e053-2991aa0ada77", "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": "54738-020", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Richmond Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "650 mg/1"}], "application_number": "part331", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20150501", "listing_expiration_date": "20261231"}