Package 0517-4002-25

Brand: papaverine hydrochloride

Generic: papaverine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0517-4002-25
Digits Only 0517400225
Product NDC 0517-4002
Product ID 0517-4002_0a4f7219-b60d-46ff-9c63-e21271569771
Description

25 VIAL in 1 CARTON (0517-4002-25) / 2 mL in 1 VIAL (0517-4002-01)

Marketing

Marketing Status
Marketed Since 1995-09-01
Brand papaverine hydrochloride
Generic papaverine hydrochloride
Sample Package No

Linked Drug Pages (1)

Papaverine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0a4f7219-b60d-46ff-9c63-e21271569771", "openfda": {"upc": ["0305174002257"], "unii": ["23473EC6BQ"], "rxcui": ["1789947"], "spl_set_id": ["9e5e2ce4-7a57-4c61-a826-64c8d11d038e"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0517-4002-25)  / 2 mL in 1 VIAL (0517-4002-01)", "package_ndc": "0517-4002-25", "marketing_start_date": "19950901"}], "brand_name": "Papaverine Hydrochloride", "product_id": "0517-4002_0a4f7219-b60d-46ff-9c63-e21271569771", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0517-4002", "generic_name": "Papaverine Hydrochloride", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Papaverine Hydrochloride", "active_ingredients": [{"name": "PAPAVERINE HYDROCHLORIDE", "strength": "30 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19950901", "listing_expiration_date": "20261231"}