sodium bicarbonate antacid

Generic: sodium bicarbonate

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate antacid
Generic Name sodium bicarbonate
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium bicarbonate 650 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-669
Product ID 71610-669_2b5b3193-1fee-30db-e063-6394a90a1f3b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2015-03-25

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 71610669
Hyphenated Format 71610-669

Supplemental Identifiers

RxCUI
198861
UNII
8MDF5V39QO

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 antacid (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
  • 60 TABLET in 1 BOTTLE (71610-669-53)
  • 90 TABLET in 1 BOTTLE (71610-669-60)
  • 180 TABLET in 1 BOTTLE (71610-669-80)
source: ndc

Packages (3)

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": "2b5b3193-1fee-30db-e063-6394a90a1f3b", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["bba7d5bf-c94b-4ee4-a399-9a2818d84c78"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-669-53)", "package_ndc": "71610-669-53", "marketing_start_date": "20221018"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-669-60)", "package_ndc": "71610-669-60", "marketing_start_date": "20221018"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-669-80)", "package_ndc": "71610-669-80", "marketing_start_date": "20221018"}], "brand_name": "Sodium Bicarbonate Antacid", "product_id": "71610-669_2b5b3193-1fee-30db-e063-6394a90a1f3b", "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": "71610-669", "generic_name": "Sodium Bicarbonate", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Bicarbonate Antacid", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "650 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150325", "listing_expiration_date": "20261231"}