narcan

Generic: naloxone hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name narcan
Generic Name naloxone hydrochloride
Labeler proficient rx lp
Dosage Form SPRAY
Routes
NASAL
Active Ingredients

naloxone hydrochloride 4 mg/.1mL

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-528
Product ID 71205-528_9f01f1ed-3bba-4243-8306-114d90da372b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA208411
Listing Expiration 2026-12-31
Marketing Start 2017-01-24

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205528
Hyphenated Format 71205-528

Supplemental Identifiers

RxCUI
1725059 1725064
UNII
F850569PQR

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 narcan (source: ndc)
Generic Name naloxone hydrochloride (source: ndc)
Application Number NDA208411 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/.1mL
source: ndc
Packaging
  • 2 VIAL, SINGLE-DOSE in 1 PACKAGE (71205-528-02) / .1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

naloxone hydrochloride (4 mg/.1mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "9f01f1ed-3bba-4243-8306-114d90da372b", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059", "1725064"], "spl_set_id": ["76b5a1ce-e601-457c-ab35-43533bba4394"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 PACKAGE (71205-528-02)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71205-528-02", "marketing_start_date": "20210203"}], "brand_name": "Narcan", "product_id": "71205-528_9f01f1ed-3bba-4243-8306-114d90da372b", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71205-528", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Narcan", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "NDA208411", "marketing_category": "NDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}