sodium bicarbonate

Generic: sodium bicarbonate

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium bicarbonate 84 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-6637
Product ID 0409-6637_f79ec8cb-b6a3-4ffb-bccf-d39f59d65621
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202494
Marketing Start 2020-07-23
Marketing End 2026-11-30

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 04096637
Hyphenated Format 0409-6637

Supplemental Identifiers

RxCUI
727995 792582
UNII
8MDF5V39QO

Packaging Origin

Original Packager
true

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 ANDA202494 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 84 mg/mL
source: ndc
Packaging
  • 10 CARTON in 1 PACKAGE (0409-6637-14) / 1 SYRINGE in 1 CARTON / 50 mL in 1 SYRINGE (0409-6637-24)
source: ndc

Packages (1)

0409-6637-14 10 CARTON in 1 PACKAGE (0409-6637-14) / 1 SYRINGE in 1 CARTON / 50 mL in 1 SYRINGE (0409-6637-24)

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": "f79ec8cb-b6a3-4ffb-bccf-d39f59d65621", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["727995", "792582"], "spl_set_id": ["ea20a5eb-641e-48cd-bcfa-74c04c45dfda"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 PACKAGE (0409-6637-14)  / 1 SYRINGE in 1 CARTON / 50 mL in 1 SYRINGE (0409-6637-24)", "package_ndc": "0409-6637-14", "marketing_end_date": "20261130", "marketing_start_date": "20200723"}], "brand_name": "Sodium Bicarbonate", "product_id": "0409-6637_f79ec8cb-b6a3-4ffb-bccf-d39f59d65621", "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": "0409-6637", "generic_name": "Sodium Bicarbonate", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA202494", "marketing_category": "ANDA", "marketing_end_date": "20261130", "marketing_start_date": "20200723"}