Package 51662-1472-1

Brand: pediatric 8.4% sodium bicarbonate

Generic: pediatric 8.4% sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 51662-1472-1
Digits Only 5166214721
Product NDC 51662-1472
Product ID 51662-1472_2b39b41d-419c-dab8-e063-6394a90a319a
Description

1 SYRINGE in 1 CARTON (51662-1472-1) / 10 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2020-01-29
Brand pediatric 8.4% sodium bicarbonate
Generic pediatric 8.4% sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

7.5% SODIUM BICARBONATE, PEDIATRIC 8.4% SODIUM BICARBONATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "2b39b41d-419c-dab8-e063-6394a90a319a", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["727995", "792577"], "spl_set_id": ["9d4bbd21-f59c-7e9c-e053-2a95a90a0826"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 CARTON (51662-1472-1)  / 10 mL in 1 SYRINGE", "package_ndc": "51662-1472-1", "marketing_start_date": "20200129"}], "brand_name": "PEDIATRIC 8.4% SODIUM BICARBONATE", "product_id": "51662-1472_2b39b41d-419c-dab8-e063-6394a90a319a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "51662-1472", "generic_name": "PEDIATRIC 8.4% SODIUM BICARBONATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PEDIATRIC 8.4% SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200129", "listing_expiration_date": "20261231"}