Package 51662-1400-1

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 51662-1400-1
Digits Only 5166214001
Product NDC 51662-1400
Product ID 51662-1400_2b378e09-dfa6-64ea-e063-6294a90ab529
Description

5 mL in 1 VIAL, SINGLE-DOSE (51662-1400-1)

Marketing

Marketing Status
Marketed Since 2019-10-19
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

SODIUM BICARBONATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2b378e09-dfa6-64ea-e063-6294a90ab529", "openfda": {"upc": ["0363323083052"], "unii": ["8MDF5V39QO"], "rxcui": ["1868469"], "spl_set_id": ["9545d58c-1c49-79b3-e053-2995a90a9d40"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, SINGLE-DOSE (51662-1400-1)", "package_ndc": "51662-1400-1", "marketing_start_date": "20191019"}], "brand_name": "SODIUM BICARBONATE", "product_id": "51662-1400_2b378e09-dfa6-64ea-e063-6294a90ab529", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "51662-1400", "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"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20191019", "listing_expiration_date": "20261231"}