sodium bicarbonate

Generic: sodium bicarbonate

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler westminster pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium bicarbonate 650 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-258
Product ID 69367-258_43b42880-bab8-4580-8a00-ae13855d44a3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2022-10-10

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367258
Hyphenated Format 69367-258

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 M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (69367-258-10)
source: ndc

Packages (1)

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

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": "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"}