naloxone hydrochloride
Generic: naloxone hydrochloride
Labeler: avkareDrug Facts
Product Profile
Brand Name
naloxone hydrochloride
Generic Name
naloxone hydrochloride
Labeler
avkare
Dosage Form
SPRAY
Routes
Active Ingredients
naloxone hydrochloride 4 mg/.1mL
Manufacturer
Identifiers & Regulatory
Product NDC
42291-493
Product ID
42291-493_485f83f8-8404-eae8-e063-6294a90a3c33
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA217992
Listing Expiration
2027-12-31
Marketing Start
2024-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42291493
Hyphenated Format
42291-493
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA217992 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/.1mL
Packaging
- 2 VIAL, SINGLE-DOSE in 1 CARTON (42291-493-02) / .1 mL in 1 VIAL, SINGLE-DOSE (42291-493-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "485f83f8-8404-eae8-e063-6294a90a3c33", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["1766a7f1-d301-945f-e063-6294a90ac6f4"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (42291-493-02) / .1 mL in 1 VIAL, SINGLE-DOSE (42291-493-01)", "package_ndc": "42291-493-02", "marketing_start_date": "20240501"}], "brand_name": "Naloxone Hydrochloride", "product_id": "42291-493_485f83f8-8404-eae8-e063-6294a90a3c33", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "42291-493", "generic_name": "Naloxone Hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA217992", "marketing_category": "ANDA", "marketing_start_date": "20240501", "listing_expiration_date": "20271231"}