Package 51662-1404-1

Brand: doxapram hydrochloride

Generic: doxapram hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1404-1
Digits Only 5166214041
Product NDC 51662-1404
Product ID 51662-1404_2b37a91d-6020-e96f-e063-6394a90a3e7a
Description

1 VIAL in 1 CARTON (51662-1404-1) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2019-10-19
Brand doxapram hydrochloride
Generic doxapram hydrochloride
Sample Package No

Linked Drug Pages (1)

DOXAPRAM HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2b37a91d-6020-e96f-e063-6394a90a3e7a", "openfda": {"unii": ["P5RU6UOQ5Y"], "rxcui": ["1047087"], "spl_set_id": ["954859c0-a121-34d6-e053-2a95a90a1e19"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (51662-1404-1)  / 20 mL in 1 VIAL", "package_ndc": "51662-1404-1", "marketing_start_date": "20191019"}], "brand_name": "DOXAPRAM HYDROCHLORIDE", "product_id": "51662-1404_2b37a91d-6020-e96f-e063-6394a90a3e7a", "dosage_form": "INJECTION", "pharm_class": ["Increased Medullary Respiratory Drive [PE]", "Respiratory Stimulant [EPC]"], "product_ndc": "51662-1404", "generic_name": "DOXAPRAM HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXAPRAM HYDROCHLORIDE", "active_ingredients": [{"name": "DOXAPRAM HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "NDA014879", "marketing_category": "NDA", "marketing_start_date": "20191019", "listing_expiration_date": "20261231"}