Package 51662-1522-1

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 51662-1522-1
Digits Only 5166215221
Product NDC 51662-1522
Product ID 51662-1522_ac0fd44a-3f3a-8d7e-e053-2995a90afeec
Description

500 mL in 1 BAG (51662-1522-1)

Marketing

Marketing Status
Marketed Since 2020-08-04
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

SODIUM CHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ac0fd44a-3f3a-8d7e-e053-2995a90afeec", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807634"], "spl_set_id": ["ac0fd44a-3f39-8d7e-e053-2995a90afeec"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (51662-1522-1)", "package_ndc": "51662-1522-1", "marketing_start_date": "20200804"}], "brand_name": "SODIUM CHLORIDE", "product_id": "51662-1522_ac0fd44a-3f3a-8d7e-e053-2995a90afeec", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1522", "generic_name": "SODIUM CHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM CHLORIDE", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "application_number": "NDA016366", "marketing_category": "NDA", "marketing_start_date": "20200804", "listing_expiration_date": "20261231"}