sodium bicarbonate 10 gr

Generic: sodium bicarbonate

Labeler: graxcell pharmaceutical, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate 10 gr
Generic Name sodium bicarbonate
Labeler graxcell pharmaceutical, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium bicarbonate 650 mg/1

Manufacturer
GRAXCELL PHARMACEUTICAL, LLC

Identifiers & Regulatory

Product NDC 70795-1190
Product ID 70795-1190_46cfbf8a-0ee3-a51f-e063-6394a90a063c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2017-10-02

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 707951190
Hyphenated Format 70795-1190

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 (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 (70795-1190-0)
  • 100 TABLET in 1 BOTTLE (70795-1190-1)
  • 200 TABLET in 1 BOTTLE (70795-1190-2)
  • 500 TABLET in 1 BOTTLE (70795-1190-5)
source: ndc

Packages (4)

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": "46cfbf8a-0ee3-a51f-e063-6394a90a063c", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["897dbb09-fb47-4e03-8cae-bf76d48a7a03"], "manufacturer_name": ["GRAXCELL PHARMACEUTICAL, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70795-1190-0)", "package_ndc": "70795-1190-0", "marketing_start_date": "20171002"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70795-1190-1)", "package_ndc": "70795-1190-1", "marketing_start_date": "20171002"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (70795-1190-2)", "package_ndc": "70795-1190-2", "marketing_start_date": "20171002"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70795-1190-5)", "package_ndc": "70795-1190-5", "marketing_start_date": "20171002"}], "brand_name": "Sodium Bicarbonate 10 gr", "product_id": "70795-1190_46cfbf8a-0ee3-a51f-e063-6394a90a063c", "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": "70795-1190", "generic_name": "Sodium Bicarbonate", "labeler_name": "GRAXCELL PHARMACEUTICAL, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Bicarbonate 10 gr", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "650 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20171002", "listing_expiration_date": "20261231"}