sodium bicarbonate
Generic: sodium bicarbonate
Labeler: apnar pharma lpDrug Facts
Product Profile
Brand Name
sodium bicarbonate
Generic Name
sodium bicarbonate
Labeler
apnar pharma lp
Dosage Form
TABLET
Routes
Active Ingredients
sodium bicarbonate 650 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
24689-137
Product ID
24689-137_08352100-b59d-c799-e063-6294a90a5e3b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M001
Listing Expiration
2026-12-31
Marketing Start
2022-06-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24689137
Hyphenated Format
24689-137
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 650 mg/1
Packaging
- 1000 TABLET in 1 BOTTLE (24689-137-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "08352100-b59d-c799-e063-6294a90a5e3b", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["e206c240-55c2-2d00-e053-2a95a90a1779"], "manufacturer_name": ["APNAR PHARMA LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (24689-137-01)", "package_ndc": "24689-137-01", "marketing_start_date": "20220624"}], "brand_name": "Sodium Bicarbonate", "product_id": "24689-137_08352100-b59d-c799-e063-6294a90a5e3b", "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": "24689-137", "generic_name": "Sodium Bicarbonate", "labeler_name": "APNAR PHARMA LP", "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": "20220624", "listing_expiration_date": "20261231"}