sodium bicarbonate 10 gr. (650 mg)

Generic: sodium bicarbonate

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

Drug Facts

Product Profile

Brand Name sodium bicarbonate 10 gr. (650 mg)
Generic Name sodium bicarbonate
Labeler gendose pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium bicarbonate 650 mg/1

Manufacturer
Gendose Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 77333-827
Product ID 77333-827_38f72774-7c52-b84f-e063-6394a90a8e64
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2023-03-14

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 77333827
Hyphenated Format 77333-827

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 10 gr. (650 mg) (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
  • 100 BLISTER PACK in 1 BOX (77333-827-10) / 1 TABLET in 1 BLISTER PACK (77333-827-25)
source: ndc

Packages (1)

Ingredients (1)

sodium bicarbonate (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38f72774-7c52-b84f-e063-6394a90a8e64", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["f6e4af32-d567-2b02-e053-6394a90aa7a0"], "manufacturer_name": ["Gendose Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX (77333-827-10)  / 1 TABLET in 1 BLISTER PACK (77333-827-25)", "package_ndc": "77333-827-10", "marketing_start_date": "20230314"}], "brand_name": "Sodium Bicarbonate 10 GR. (650 MG)", "product_id": "77333-827_38f72774-7c52-b84f-e063-6394a90a8e64", "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": "77333-827", "generic_name": "Sodium Bicarbonate", "labeler_name": "Gendose Pharmaceuticals, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Bicarbonate", "brand_name_suffix": "10 GR. (650 MG)", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "650 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230314", "listing_expiration_date": "20261231"}