sodium bicarbonate
Generic: sodium bicarbonate
Labeler: medical purchasing solutions, llcDrug Facts
Product Profile
Brand Name
sodium bicarbonate
Generic Name
sodium bicarbonate
Labeler
medical purchasing solutions, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium bicarbonate 84 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71872-7310
Product ID
71872-7310_09cfad01-259c-fa43-e063-6394a90ad5a1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211091
Listing Expiration
2026-12-31
Marketing Start
2019-08-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
718727310
Hyphenated Format
71872-7310
Supplemental Identifiers
RxCUI
UNII
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
ANDA211091 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 84 mg/mL
Packaging
- 1 VIAL in 1 BAG (71872-7310-1) / 50 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "09cfad01-259c-fa43-e063-6394a90ad5a1", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["09cf38c2-0b44-eca1-e063-6294a90a72d8"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (71872-7310-1) / 50 mL in 1 VIAL", "package_ndc": "71872-7310-1", "marketing_start_date": "20230920"}], "brand_name": "Sodium Bicarbonate", "product_id": "71872-7310_09cfad01-259c-fa43-e063-6394a90ad5a1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "71872-7310", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA211091", "marketing_category": "ANDA", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}