sodium bicarbonate

Generic: sodium bicarbonate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler a-s medication solutions
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium bicarbonate 84 mg/mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6813
Product ID 50090-6813_132e1b7b-c63c-43d3-ac31-8ca034f1210f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211091
Listing Expiration 2026-12-31
Marketing Start 2019-08-01

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906813
Hyphenated Format 50090-6813

Supplemental Identifiers

RxCUI
1868486
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 (source: ndc)
Generic Name sodium bicarbonate (source: ndc)
Application Number ANDA211091 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 84 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (50090-6813-0) / 50 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

sodium bicarbonate (84 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "132e1b7b-c63c-43d3-ac31-8ca034f1210f", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["d89406d3-4356-4a8c-acc1-89efe1d27010"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (50090-6813-0)  / 50 mL in 1 VIAL", "package_ndc": "50090-6813-0", "marketing_start_date": "20231108"}], "brand_name": "Sodium Bicarbonate", "product_id": "50090-6813_132e1b7b-c63c-43d3-ac31-8ca034f1210f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "50090-6813", "generic_name": "SODIUM BICARBONATE", "labeler_name": "A-S Medication Solutions", "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"}