Package 51754-0102-4

Brand: zinc chloride

Generic: zinc chloride
NDC Package

Package Facts

Identity

Package NDC 51754-0102-4
Digits Only 5175401024
Product NDC 51754-0102
Product ID 51754-0102_5f09a6b3-abb1-4d80-9ed9-88a343ea472b
Description

25 VIAL in 1 CARTON (51754-0102-4) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2021-08-27
Brand zinc chloride
Generic zinc chloride
Sample Package No

Linked Drug Pages (1)

Zinc Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "5f09a6b3-abb1-4d80-9ed9-88a343ea472b", "openfda": {"unii": ["86Q357L16B"], "rxcui": ["237508"], "spl_set_id": ["2bd646d2-2a2a-4376-8da0-c7f08b0511ac"], "manufacturer_name": ["Exela Pharma Sciences,LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (51754-0102-4)  / 10 mL in 1 VIAL", "package_ndc": "51754-0102-4", "marketing_start_date": "20210827"}], "brand_name": "Zinc Chloride", "product_id": "51754-0102_5f09a6b3-abb1-4d80-9ed9-88a343ea472b", "dosage_form": "INJECTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "51754-0102", "generic_name": "Zinc Chloride", "labeler_name": "Exela Pharma Sciences,LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zinc Chloride", "active_ingredients": [{"name": "ZINC CHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA212007", "marketing_category": "ANDA", "marketing_start_date": "20210827", "listing_expiration_date": "20261231"}