sodium bicarbonate

Generic: sodium bicarbonate

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium bicarbonate 42 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1497
Product ID 51662-1497_2b389f01-ff73-4db6-e063-6394a90aae4a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202981
Listing Expiration 2026-12-31
Marketing Start 2020-02-18

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621497
Hyphenated Format 51662-1497

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
  • 5 mL in 1 VIAL, SINGLE-USE (51662-1497-1)
source: ndc

Packages (1)

51662-1497-1 5 mL in 1 VIAL, SINGLE-USE (51662-1497-1)

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": "2b389f01-ff73-4db6-e063-6394a90aae4a", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868469"], "spl_set_id": ["9ee46a5b-d00e-4254-e053-2995a90aeb3a"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, SINGLE-USE (51662-1497-1)", "package_ndc": "51662-1497-1", "marketing_start_date": "20200218"}], "brand_name": "SODIUM BICARBONATE", "product_id": "51662-1497_2b389f01-ff73-4db6-e063-6394a90aae4a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "51662-1497", "generic_name": "SODIUM BICARBONATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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": "20200218", "listing_expiration_date": "20261231"}