Package 70069-526-25

Brand: zinc chloride

Generic: zinc chloride
NDC Package

Package Facts

Identity

Package NDC 70069-526-25
Digits Only 7006952625
Product NDC 70069-526
Description

25 VIAL, PLASTIC in 1 CARTON (70069-526-25) / 10 mL in 1 VIAL, PLASTIC (70069-526-01)

Marketing

Marketing Status
Marketed Since 2024-10-16
Brand zinc chloride
Generic zinc chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6b701c2f-faba-4d1a-ad8d-bebaf0ec7cfa", "openfda": {"upc": ["0370069526019"], "unii": ["86Q357L16B"], "rxcui": ["237508"], "spl_set_id": ["9a4f7a7b-26d0-4292-bc7b-6ca9fa48600f"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, PLASTIC in 1 CARTON (70069-526-25)  / 10 mL in 1 VIAL, PLASTIC (70069-526-01)", "package_ndc": "70069-526-25", "marketing_start_date": "20241016"}], "brand_name": "Zinc Chloride", "product_id": "70069-526_6b701c2f-faba-4d1a-ad8d-bebaf0ec7cfa", "dosage_form": "INJECTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "70069-526", "generic_name": "Zinc Chloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zinc Chloride", "active_ingredients": [{"name": "ZINC CHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA216152", "marketing_category": "ANDA", "marketing_start_date": "20241016", "listing_expiration_date": "20261231"}