Package 51662-1497-1

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 51662-1497-1
Digits Only 5166214971
Product NDC 51662-1497
Description

5 mL in 1 VIAL, SINGLE-USE (51662-1497-1)

Marketing

Marketing Status
Marketed Since 2020-02-18
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2b389f01-ff73-4db6-e063-6394a90aae4a", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868469"], "spl_set_id": ["9ee46a5b-d00e-4254-e053-2995a90aeb3a"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, SINGLE-USE (51662-1497-1)", "package_ndc": "51662-1497-1", "marketing_start_date": "20200218"}], "brand_name": "SODIUM BICARBONATE", "product_id": "51662-1497_2b389f01-ff73-4db6-e063-6394a90aae4a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "51662-1497", "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": "42 mg/mL"}], "application_number": "ANDA202981", "marketing_category": "ANDA", "marketing_start_date": "20200218", "listing_expiration_date": "20261231"}