Package 51662-1577-1

Brand: 0.9% sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 51662-1577-1
Digits Only 5166215771
Product NDC 51662-1577
Product ID 51662-1577_c755e41b-acbb-7234-e053-2995a90aff0f
Description

500 mL in 1 BAG (51662-1577-1)

Marketing

Marketing Status
Marketed Since 2021-07-17
Brand 0.9% sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

0.9% SODIUM CHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c755e41b-acbb-7234-e053-2995a90aff0f", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807634"], "spl_set_id": ["c755e41b-acba-7234-e053-2995a90aff0f"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (51662-1577-1)", "package_ndc": "51662-1577-1", "marketing_start_date": "20210717"}], "brand_name": "0.9% SODIUM CHLORIDE", "product_id": "51662-1577_c755e41b-acbb-7234-e053-2995a90aff0f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "51662-1577", "generic_name": "SODIUM CHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "0.9% SODIUM CHLORIDE", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "ANDA207310", "marketing_category": "ANDA", "marketing_start_date": "20210717", "listing_expiration_date": "20261231"}