sodium bicarbonate 10 gr (650 mg)

Generic: sodium bicarbonate

Labeler: advanced rx 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 advanced rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium bicarbonate 650 mg/1

Manufacturer
Advanced Rx LLC

Identifiers & Regulatory

Product NDC 80513-611
Product ID 80513-611_3d912fde-5c7a-e74c-e063-6394a90a6e1f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2025-09-01

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 80513611
Hyphenated Format 80513-611

Supplemental Identifiers

RxCUI
198861
UPC
0380513001849
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
  • 200 TABLET in 1 BOTTLE (80513-611-02)
source: ndc

Packages (1)

80513-611-02 200 TABLET in 1 BOTTLE (80513-611-02)

Ingredients (1)

sodium bicarbonate (650 mg/1)

Linked Drug Pages (1)

Sodium Bicarbonate 10 GR (650 MG) ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3d912fde-5c7a-e74c-e063-6394a90a6e1f", "openfda": {"upc": ["0380513001849"], "unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["634e8d52-6d04-42f9-98f6-2634473b5dfd"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (80513-611-02)", "package_ndc": "80513-611-02", "marketing_start_date": "20250901"}], "brand_name": "Sodium Bicarbonate 10 GR (650 MG)", "product_id": "80513-611_3d912fde-5c7a-e74c-e063-6394a90a6e1f", "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": "80513-611", "generic_name": "Sodium Bicarbonate", "labeler_name": "Advanced Rx 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": "20250901", "listing_expiration_date": "20261231"}