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 0409-6625
Product ID 0409-6625_55e7a069-73d0-45e3-8d36-f307f5802443
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202432
Listing Expiration 2026-12-31
Marketing Start 2020-10-15

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 04096625
Hyphenated Format 0409-6625

Supplemental Identifiers

RxCUI
1868486
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 ANDA202432 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 84 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6625-35) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-6625-30)
source: ndc

Packages (1)

0409-6625-35 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6625-35) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-6625-30)

Ingredients (1)

sodium bicarbonate (84 mg/mL)

Linked Drug Pages (2)

Sodium Bicarbonate ndc-match (0.9) SODIUM BICARBONATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "55e7a069-73d0-45e3-8d36-f307f5802443", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["8664c7ce-707b-4c6c-9ce4-7160b5f877f8"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6625-35)  / 50 mL in 1 VIAL, SINGLE-DOSE (0409-6625-30)", "package_ndc": "0409-6625-35", "marketing_start_date": "20201015"}], "brand_name": "Sodium Bicarbonate", "product_id": "0409-6625_55e7a069-73d0-45e3-8d36-f307f5802443", "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": "0409-6625", "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": "ANDA202432", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}