Package 14789-121-05

Brand: papaverine hydrochloride

Generic: papaverine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 14789-121-05
Digits Only 1478912105
Product NDC 14789-121
Product ID 14789-121_28dc648b-5306-8daf-e063-6294a90a9b44
Description

10 VIAL, SINGLE-USE in 1 CARTON (14789-121-05) / 2 mL in 1 VIAL, SINGLE-USE (14789-121-07)

Marketing

Marketing Status
Marketed Since 2021-06-28
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "28dc648b-5306-8daf-e063-6294a90a9b44", "openfda": {"unii": ["23473EC6BQ"], "rxcui": ["1789947"], "spl_set_id": ["1e76839f-82eb-42a8-abc2-e7fbc533082d"], "manufacturer_name": ["Nexus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (14789-121-05)  / 2 mL in 1 VIAL, SINGLE-USE (14789-121-07)", "package_ndc": "14789-121-05", "marketing_start_date": "20210628"}], "brand_name": "Papaverine Hydrochloride", "product_id": "14789-121_28dc648b-5306-8daf-e063-6294a90a9b44", "dosage_form": "INJECTION", "product_ndc": "14789-121", "generic_name": "Papaverine Hydrochloride", "labeler_name": "Nexus Pharmaceuticals, LLC", "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": "20210628", "listing_expiration_date": "20261231"}