Package 0641-6018-01

Brand: dopram

Generic: doxapram hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-6018-01
Digits Only 0641601801
Product NDC 0641-6018
Product ID 0641-6018_ccb9f1b7-b7b1-4db2-b5db-093d147529a7
Description

20 mL in 1 VIAL (0641-6018-01)

Marketing

Marketing Status
Marketed Since 1965-06-23
Brand dopram
Generic doxapram hydrochloride
Sample Package No

Linked Drug Pages (1)

Dopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ccb9f1b7-b7b1-4db2-b5db-093d147529a7", "openfda": {"unii": ["P5RU6UOQ5Y"], "rxcui": ["1047087", "1047511"], "spl_set_id": ["b8eb330a-a75b-46cb-b694-5be9327ed2eb"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL (0641-6018-01)", "package_ndc": "0641-6018-01", "marketing_start_date": "19650623"}, {"sample": false, "description": "6 VIAL in 1 CARTON (0641-6018-06)  / 20 mL in 1 VIAL (0641-6018-01)", "package_ndc": "0641-6018-06", "marketing_start_date": "19650623"}], "brand_name": "Dopram", "product_id": "0641-6018_ccb9f1b7-b7b1-4db2-b5db-093d147529a7", "dosage_form": "INJECTION", "pharm_class": ["Increased Medullary Respiratory Drive [PE]", "Respiratory Stimulant [EPC]"], "product_ndc": "0641-6018", "generic_name": "Doxapram hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dopram", "active_ingredients": [{"name": "DOXAPRAM HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "NDA014879", "marketing_category": "NDA", "marketing_start_date": "19650623", "listing_expiration_date": "20261231"}