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 42 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-5555
Product ID 0409-5555_e3a44e63-8594-40b6-a3fa-d135b3149661
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202981
Listing Expiration 2027-12-31
Marketing Start 2020-08-26

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04095555
Hyphenated Format 0409-5555

Supplemental Identifiers

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 ANDA202981 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 42 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-01) / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-11)
source: ndc

Packages (1)

Ingredients (1)

sodium bicarbonate (42 mg/mL)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e3a44e63-8594-40b6-a3fa-d135b3149661", "openfda": {"unii": ["8MDF5V39QO"], "spl_set_id": ["0c24b592-4bc8-456f-acac-9c9525844a06"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-01)  / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-11)", "package_ndc": "0409-5555-01", "marketing_start_date": "20200826"}], "brand_name": "Sodium Bicarbonate", "product_id": "0409-5555_e3a44e63-8594-40b6-a3fa-d135b3149661", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "0409-5555", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "42 mg/mL"}], "application_number": "ANDA202981", "marketing_category": "ANDA", "marketing_start_date": "20200826", "listing_expiration_date": "20271231"}