NDC 51662-1404

DOXAPRAM HYDROCHLORIDE

Doxapram Hydrochloride

DOXAPRAM HYDROCHLORIDE is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co Llc, Dba Healthfirst. The primary component is Doxapram Hydrochloride.

• Product ID: 51662-1404_954859c0-a122-34d6-e053-2a95a90a1e19
• NDC: 51662-1404
• Product Type: Human Prescription Drug
• Proprietary Name: DOXAPRAM HYDROCHLORIDE
• Generic Name: Doxapram Hydrochloride
• Dosage Form: Injection
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2019-10-19
• Marketing Category: NDA / NDA
• Application Number: NDA014879
• Labeler Name: HF Acquisition Co LLC, DBA HealthFirst
• Substance Name: DOXAPRAM HYDROCHLORIDE
• Active Ingredient Strength: 20 mg/mL
• Pharm Classes: Increased Medullary Respiratory Drive [PE],Respiratory Stimulant [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 51662-1404-1

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

• Marketing Start Date: 2019-10-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51662-1404-1 [51662140401]

DOXAPRAM HYDROCHLORIDE INJECTION

• Marketing Category: NDA
• Application Number: NDA014879
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-10-19

Drug Details

Active Ingredients

Ingredient	Strength
DOXAPRAM HYDROCHLORIDE	20 mg/mL

Pharmacological Class

• Increased Medullary Respiratory Drive [PE]
• Respiratory Stimulant [EPC]

NDC Crossover Matching brand name "DOXAPRAM HYDROCHLORIDE" or generic name "Doxapram Hydrochloride"

NDC	Brand Name	Generic Name
51662-1404	DOXAPRAM HYDROCHLORIDE	DOXAPRAM HYDROCHLORIDE
0641-6018	Dopram	Doxapram hydrochloride