doxapram hydrochloride

Generic: doxapram hydrochloride

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxapram hydrochloride
Generic Name doxapram hydrochloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

doxapram hydrochloride 20 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1404
Product ID 51662-1404_2b37a91d-6020-e96f-e063-6394a90a3e7a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA014879
Listing Expiration 2026-12-31
Marketing Start 2019-10-19

Pharmacologic Class

Classes
increased medullary respiratory drive [pe] respiratory stimulant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621404
Hyphenated Format 51662-1404

Supplemental Identifiers

RxCUI
1047087
UNII
P5RU6UOQ5Y

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name doxapram hydrochloride (source: ndc)
Generic Name doxapram hydrochloride (source: ndc)
Application Number NDA014879 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (51662-1404-1) / 20 mL in 1 VIAL
source: ndc

Packages (1)

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

Ingredients (1)

doxapram hydrochloride (20 mg/mL)

Linked Drug Pages (1)

DOXAPRAM HYDROCHLORIDE ndc-match (0.9)

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"}