Home NDC 51662-1310 INFANT 4.2% SODIUM BICARBONATE
Product NDC 51662-1310
11-digit product format 516621310
Labeler code 51662
Product ID 51662-1310_37b6930c-c88f-4fd7-e063-6394a90a37f1
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name INFANT 4.2% SODIUM BICARBONATE
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler HF Acquisition Co LLC, DBA HealthFirst
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2018-10-21
Substance SODIUM BICARBONATE
Active strength 42 mg/mL
Pharmacologic classes Alkalinizing Activity [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base INFANT 4.2% SODIUM BICARBONATE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BICARBONATE 42 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 1868473 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51662-1310-1 INFANT 4.2% SODIUM BICARBONATE 10 mL in 1 SYRINGE INJECTION, SOLUTION 10 8 51662-1310-2 INFANT 4.2% SODIUM BICARBONATE 1 in 1 POUCH INJECTION, SOLUTION 1 8 51662-1310-2 INFANT 4.2% SODIUM BICARBONATE 1 in 1 CARTON INJECTION, SOLUTION 1 8 51662-1310-3 INFANT 4.2% SODIUM BICARBONATE 10 in 1 CASE INJECTION, SOLUTION 10 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51662-1310 INFANT 4.2% SODIUM BICARBONATE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] 7 Current NDC, Legacy NDC, 4 package rows 20240517_78c25911-0042-664e-e053-2a91aa0a57a1.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 51662-1310-1 51662131001 10 mL in 1 SYRINGE (51662-1310-1) 10 ml 2018-10-21 0000-00-00 No No Current 51662-1310-2 51662131002 1 in 1 POUCH Historical 51662-1310-3 51662131003 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 10 pouch 2023-01-09 No No Current