naloxone hydrochloride

Generic: naloxone hydrochloride

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naloxone hydrochloride
Generic Name naloxone hydrochloride
Labeler redpharm drug
Dosage Form SPRAY, METERED
Routes
NASAL
Active Ingredients

naloxone hydrochloride 4 mg/.1mL

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-1928
Product ID 67296-1928_46e9401c-067d-0ed9-e063-6294a90aca49
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209522
Marketing Start 2021-12-22
Marketing End 2026-06-30

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672961928
Hyphenated Format 67296-1928

Supplemental Identifiers

RxCUI
1725059
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 naloxone hydrochloride (source: ndc)
Generic Name naloxone hydrochloride (source: ndc)
Application Number ANDA209522 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/.1mL
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (67296-1928-2) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK / .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": "46e9401c-067d-0ed9-e063-6294a90aca49", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["2fc0a205-6075-6253-e063-6294a90ad2df"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (67296-1928-2)  / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "67296-1928-2", "marketing_end_date": "20260630", "marketing_start_date": "20211222"}], "brand_name": "Naloxone Hydrochloride", "product_id": "67296-1928_46e9401c-067d-0ed9-e063-6294a90aca49", "dosage_form": "SPRAY, METERED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "67296-1928", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA209522", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20211222"}