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 50090-0530
Product ID 50090-0530_b29cb3b6-4913-49b3-82a2-590b1792703a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202432
Listing Expiration 2026-12-31
Marketing Start 2021-03-01

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 500900530
Hyphenated Format 50090-0530

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 ANDA202432 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 84 mg/mL
source: ndc
Packaging
  • 50 mL in 1 VIAL (50090-0530-0)
source: ndc

Packages (1)

50090-0530-0 50 mL in 1 VIAL (50090-0530-0)

Ingredients (1)

sodium bicarbonate (84 mg/mL)

Linked Drug Pages (1)

Sodium Bicarbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "b29cb3b6-4913-49b3-82a2-590b1792703a", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["619cb558-84e5-43ea-91e9-28c764f9f9c0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL (50090-0530-0)", "package_ndc": "50090-0530-0", "marketing_start_date": "20210301"}], "brand_name": "Sodium Bicarbonate", "product_id": "50090-0530_b29cb3b6-4913-49b3-82a2-590b1792703a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "50090-0530", "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": "ANDA202432", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}