# DOXAPRAM HYDROCHLORIDE

NDC: 51662-1404
Generic name: DOXAPRAM HYDROCHLORIDE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20191019

FDA application: NDA014879

## Active ingredients

- DOXAPRAM HYDROCHLORIDE: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1404"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1404
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=954859c0-a121-34d6-e053-2a95a90a1e19