dopram

Generic: doxapram hydrochloride

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name dopram
Generic Name doxapram hydrochloride
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

doxapram hydrochloride 20 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0641-6018
Product ID 0641-6018_ccb9f1b7-b7b1-4db2-b5db-093d147529a7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA014879
Listing Expiration 2026-12-31
Marketing Start 1965-06-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06416018
Hyphenated Format 0641-6018

Supplemental Identifiers

RxCUI
1047087 1047511
UNII
P5RU6UOQ5Y

Packaging Origin

Original Packager
true

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 dopram (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
  • 20 mL in 1 VIAL (0641-6018-01)
  • 6 VIAL in 1 CARTON (0641-6018-06) / 20 mL in 1 VIAL (0641-6018-01)
source: ndc

Packages (2)

0641-6018-01 20 mL in 1 VIAL (0641-6018-01) 0641-6018-06 6 VIAL in 1 CARTON (0641-6018-06) / 20 mL in 1 VIAL (0641-6018-01)

Ingredients (1)

doxapram hydrochloride (20 mg/mL)

Linked Drug Pages (1)

Dopram ndc-match (0.9)

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"}