Home NDC 51662-1573 SODIUM BICARBONATE
Product NDC 51662-1573
11-digit product format 516621573
Labeler code 51662
Product ID 51662-1573_4db6ff50-e973-9770-e063-6394a90a1793
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name SODIUM BICARBONATE
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler HF Acquisition Co LLC, DBA HealthFirst
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-02-18
Substance SODIUM BICARBONATE
Active strength 84 mg/mL
Pharmacologic classes Alkalinizing Activity [MoA]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base SODIUM BICARBONATE
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BICARBONATE 84 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8MDF5V39QO Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1868486 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51662-1573-1 SODIUM BICARBONATE 50 mL in 1 VIAL, SINGLE-DOSE INJECTION, SOLUTION 50 4 51662-1573-2 SODIUM BICARBONATE 50 mL in 1 VIAL, SINGLE-DOSE INJECTION, SOLUTION 50 4 51662-1573-2 SODIUM BICARBONATE 1 in 1 POUCH INJECTION, SOLUTION 1 4 51662-1573-3 SODIUM BICARBONATE 25 in 1 CASE INJECTION, SOLUTION 25 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51662-1573 SODIUM BICARBONATE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] 3 Current NDC, Legacy NDC, 4 package rows 20240201_d8516f38-6f92-32d1-e053-2995a90a96bf.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 51662-1573-1 51662157301 50 mL in 1 VIAL, SINGLE-DOSE (51662-1573-1) 50 ml 2022-02-18 0000-00-00 No No Current 51662-1573-2 51662157302 50 mL in 1 VIAL, SINGLE-DOSE 50 ml Historical 51662-1573-3 51662157303 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 25 pouch 2022-07-31 0000-00-00 No No Current