sodium bicarbonate

Generic: sodium bicarbonate

Labeler: richmond pharmaceuticals, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler richmond pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium bicarbonate 650 mg/1

Manufacturer
Richmond Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 54738-020
Product ID 54738-020_5cc6cec2-9f03-6cf9-e053-2991aa0ada77
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH FINAL
Application Number part331
Listing Expiration 2026-12-31
Marketing Start 2015-05-01

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 54738020
Hyphenated Format 54738-020

Supplemental Identifiers

RxCUI
198861
UNII
8MDF5V39QO

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sodium bicarbonate (source: ndc)
Generic Name sodium bicarbonate (source: ndc)
Application Number part331 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE, PLASTIC (54738-020-03)
source: ndc

Packages (1)

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

Ingredients (1)

sodium bicarbonate (650 mg/1)

Linked Drug Pages (1)

SODIUM BICARBONATE ndc-match (0.9)

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"}