Package 51662-1573-1

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 51662-1573-1
Digits Only 5166215731
Product NDC 51662-1573
Description

50 mL in 1 VIAL, SINGLE-DOSE (51662-1573-1)

Marketing

Marketing Status
Marketed Since 2022-02-18
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": "103601ca-3a9c-74c4-e063-6294a90a524c", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["d8516f38-6f92-32d1-e053-2995a90a96bf"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, SINGLE-DOSE (51662-1573-1)", "package_ndc": "51662-1573-1", "marketing_start_date": "20220218"}, {"sample": false, "description": "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", "package_ndc": "51662-1573-3", "marketing_start_date": "20220731"}], "brand_name": "SODIUM BICARBONATE", "product_id": "51662-1573_103601ca-3a9c-74c4-e063-6294a90a524c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "51662-1573", "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": "84 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20220218", "listing_expiration_date": "20261231"}