NDC 51662-1463

7.5% SODIUM BICARBONATE

7.5% Sodium Bicarbonate

7.5% SODIUM BICARBONATE is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co Llc, Dba Healthfirst. The primary component is Sodium Bicarbonate.

Product ID51662-1463_9d4bbd21-f59d-7e9c-e053-2a95a90a0826
NDC51662-1463
Product TypeHuman Prescription Drug
Proprietary Name7.5% SODIUM BICARBONATE
Generic Name7.5% Sodium Bicarbonate
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2020-01-29
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameHF Acquisition Co LLC, DBA HealthFirst
Substance NameSODIUM BICARBONATE
Active Ingredient Strength75 mg/mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 51662-1463-1

1 SYRINGE in 1 CARTON (51662-1463-1) > 50 mL in 1 SYRINGE
Marketing Start Date2020-01-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51662-1463-1 [51662146301]

7.5% SODIUM BICARBONATE INJECTION, SOLUTION
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-01-29

Drug Details

Active Ingredients

IngredientStrength
SODIUM BICARBONATE75 mg/mL

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.