infant 4.2% sodium bicarbonate

Generic: infant 4.2% sodium bicarbonate

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

Drug Facts

Product Profile

Brand Name infant 4.2% sodium bicarbonate
Generic Name infant 4.2% 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 51662-1310
Product ID 51662-1310_37b6930c-c88f-4fd7-e063-6394a90a37f1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2018-10-21

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621310
Hyphenated Format 51662-1310

Supplemental Identifiers

RxCUI
1868473
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 infant 4.2% sodium bicarbonate (source: ndc)
Generic Name infant 4.2% sodium bicarbonate (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 42 mg/mL
source: ndc
Packaging
  • 10 mL in 1 SYRINGE (51662-1310-1)
  • 10 POUCH in 1 CASE (51662-1310-3) / 1 CARTON in 1 POUCH (51662-1310-2) / 1 SYRINGE in 1 CARTON / 10 mL in 1 SYRINGE
source: ndc

Packages (2)

Ingredients (1)

sodium bicarbonate (42 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "37b6930c-c88f-4fd7-e063-6394a90a37f1", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868473"], "spl_set_id": ["78c25911-0042-664e-e053-2a91aa0a57a1"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 SYRINGE (51662-1310-1)", "package_ndc": "51662-1310-1", "marketing_start_date": "20181021"}, {"sample": false, "description": "10 POUCH in 1 CASE (51662-1310-3)  / 1 CARTON in 1 POUCH (51662-1310-2)  / 1 SYRINGE in 1 CARTON / 10 mL in 1 SYRINGE", "package_ndc": "51662-1310-3", "marketing_start_date": "20230109"}], "brand_name": "INFANT 4.2% SODIUM BICARBONATE", "product_id": "51662-1310_37b6930c-c88f-4fd7-e063-6394a90a37f1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "51662-1310", "generic_name": "INFANT 4.2% SODIUM BICARBONATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "INFANT 4.2% SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "42 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20181021", "listing_expiration_date": "20261231"}