Package 0409-4350-03

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0409-4350-03
Digits Only 0409435003
Product NDC 0409-4350
Product ID 0409-4350_18648c0d-5f60-4195-92f0-1dffc1452d4c
Description

10 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-4350-03) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0409-4350-13)

Marketing

Marketing Status
Marketed Since 2005-04-30
Brand diltiazem hydrochloride
Generic diltiazem hydrochloride
Sample Package No

Linked Drug Pages (1)

Diltiazem Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "18648c0d-5f60-4195-92f0-1dffc1452d4c", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["1791230", "1791240"], "spl_set_id": ["bba03666-ff4f-4bf6-fa92-78e1ec2d9073"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-4350-03)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0409-4350-13)", "package_ndc": "0409-4350-03", "marketing_start_date": "20050430"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "0409-4350_18648c0d-5f60-4195-92f0-1dffc1452d4c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]"], "product_ndc": "0409-4350", "generic_name": "DILTIAZEM HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA075853", "marketing_category": "ANDA", "marketing_start_date": "20050430", "listing_expiration_date": "20261231"}