Package 51662-1342-1

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 51662-1342-1
Digits Only 5166213421
Product NDC 51662-1342
Product ID 51662-1342_2b39e554-da97-1979-e063-6394a90a887a
Description

10 mL in 1 VIAL, SINGLE-DOSE (51662-1342-1)

Marketing

Marketing Status
Marketed Since 2018-12-22
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": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2b39e554-da97-1979-e063-6394a90a887a", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807637"], "spl_set_id": ["7da788fc-3481-527f-e053-2a91aa0af6ac"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (51662-1342-1)", "package_ndc": "51662-1342-1", "marketing_start_date": "20181222"}], "brand_name": "SODIUM CHLORIDE", "product_id": "51662-1342_2b39e554-da97-1979-e063-6394a90a887a", "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": "51662-1342", "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": "9 mg/mL"}], "application_number": "NDA018803", "marketing_category": "NDA", "marketing_start_date": "20181222", "listing_expiration_date": "20261231"}