Package 0781-6021-94

Brand: diluent

Generic: water solution
NDC Package

Package Facts

Identity

Package NDC 0781-6021-94
Digits Only 0781602194
Product NDC 0781-6021
Description

1 VIAL in 1 CARTON (0781-6021-94) / 50 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2019-03-25
Brand diluent
Generic water solution
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "fe80d00e-9eba-4192-9515-f9a5ad686a53", "openfda": {"nui": ["N0000175416", "M0017817", "N0000009909"], "unii": ["059QF0KO0R", "RUM6K67ESG"], "rxcui": ["349407", "349408", "349409", "349410"], "spl_set_id": ["473297ca-a872-4052-a053-87dc8f0d3c13"], "pharm_class_cs": ["Prostaglandins I [CS]"], "pharm_class_pe": ["Vasodilation [PE]"], "pharm_class_epc": ["Prostacycline Vasodilator [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0781-6021-94)  / 50 mL in 1 VIAL", "package_ndc": "0781-6021-94", "marketing_start_date": "20190325"}], "brand_name": "DILUENT", "product_id": "0781-6021_fe80d00e-9eba-4192-9515-f9a5ad686a53", "dosage_form": "INJECTION", "product_ndc": "0781-6021", "generic_name": "water solution", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DILUENT", "active_ingredients": [{"name": "WATER", "strength": "1 mL/mL"}], "application_number": "ANDA203649", "marketing_category": "ANDA", "marketing_start_date": "20190325", "listing_expiration_date": "20261231"}