sodium bicarbonate

Generic: sodium bicarbonate

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

Drug Facts

Product Profile

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

sodium bicarbonate 42 mg/mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9951
Product ID 0404-9951_1cc6a0c6-0475-4c98-92ab-a6184974cfd7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202981
Listing Expiration 2026-12-31
Marketing Start 2022-01-12

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 04049951
Hyphenated Format 0404-9951

Supplemental Identifiers

RxCUI
1868469
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 ANDA202981 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 42 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-USE in 1 BAG (0404-9951-05) / 5 mL in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

0404-9951-05 1 VIAL, SINGLE-USE in 1 BAG (0404-9951-05) / 5 mL in 1 VIAL, SINGLE-USE

Ingredients (1)

sodium bicarbonate (42 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": "1cc6a0c6-0475-4c98-92ab-a6184974cfd7", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868469"], "spl_set_id": ["da484a2f-154f-48b4-8467-7a86729204c3"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 BAG (0404-9951-05)  / 5 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0404-9951-05", "marketing_start_date": "20220112"}], "brand_name": "SODIUM BICARBONATE", "product_id": "0404-9951_1cc6a0c6-0475-4c98-92ab-a6184974cfd7", "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": "0404-9951", "generic_name": "sodium bicarbonate", "labeler_name": "Henry Schein, 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": "20220112", "listing_expiration_date": "20261231"}