sodium bicarbonate
Generic: sodium bicarbonate
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
sodium bicarbonate
Generic Name
sodium bicarbonate
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium bicarbonate 84 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1573
Product ID
51662-1573_103601ca-3a9c-74c4-e063-6294a90a524c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2022-02-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621573
Hyphenated Format
51662-1573
Supplemental Identifiers
RxCUI
UNII
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)
Routes
source: ndc
Resolved Composition
Strengths
- 84 mg/mL
Packaging
- 50 mL in 1 VIAL, SINGLE-DOSE (51662-1573-1)
- 25 POUCH in 1 CASE (51662-1573-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1573-2) / 50 mL in 1 VIAL, SINGLE-DOSE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "103601ca-3a9c-74c4-e063-6294a90a524c", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["d8516f38-6f92-32d1-e053-2995a90a96bf"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, SINGLE-DOSE (51662-1573-1)", "package_ndc": "51662-1573-1", "marketing_start_date": "20220218"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1573-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1573-2) / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1573-3", "marketing_start_date": "20220731"}], "brand_name": "SODIUM BICARBONATE", "product_id": "51662-1573_103601ca-3a9c-74c4-e063-6294a90a524c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "51662-1573", "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": "84 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20220218", "listing_expiration_date": "20261231"}