sodium bicarbonate

Generic: sodium bicarbonate

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium bicarbonate 650 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7261
Product ID 0904-7261_289e96ec-d8d1-ee93-e063-6394a90a38d7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2022-10-26

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 09047261
Hyphenated Format 0904-7261

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
  • 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-7261-61) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7261-61 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-7261-61) / 10 TABLET in 1 BLISTER PACK

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": "289e96ec-d8d1-ee93-e063-6394a90a38d7", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["ebf340c9-0b6d-13d2-e053-2995a90ae338"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-7261-61)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7261-61", "marketing_start_date": "20221026"}], "brand_name": "Sodium Bicarbonate", "product_id": "0904-7261_289e96ec-d8d1-ee93-e063-6394a90a38d7", "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": "0904-7261", "generic_name": "Sodium Bicarbonate", "labeler_name": "Major Pharmaceuticals", "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": "20221026", "listing_expiration_date": "20261231"}