naloxone hydrochloride

Generic: naloxone hydrochloride

Labeler: cvs pharmacy, inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naloxone hydrochloride
Generic Name naloxone hydrochloride
Labeler cvs pharmacy, inc
Dosage Form SPRAY
Routes
NASAL
Active Ingredients

naloxone hydrochloride 4 mg/.1mL

Manufacturer
CVS Pharmacy, Inc

Identifiers & Regulatory

Product NDC 51316-210
Product ID 51316-210_3c18b06c-be22-4076-84f8-80610dda1e61
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA217992
Listing Expiration 2027-12-31
Marketing Start 2024-04-24

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51316210
Hyphenated Format 51316-210

Supplemental Identifiers

RxCUI
1725059
UPC
0050428443958
UNII
F850569PQR

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 naloxone hydrochloride (source: ndc)
Generic Name naloxone hydrochloride (source: ndc)
Application Number ANDA217992 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/.1mL
source: ndc
Packaging
  • 2 VIAL in 1 CARTON (51316-210-02) / .1 mL in 1 VIAL (51316-210-01)
source: ndc

Packages (1)

51316-210-02 2 VIAL in 1 CARTON (51316-210-02) / .1 mL in 1 VIAL (51316-210-01)

Ingredients (1)

naloxone hydrochloride (4 mg/.1mL)

Linked Drug Pages (1)

Naloxone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "3c18b06c-be22-4076-84f8-80610dda1e61", "openfda": {"upc": ["0050428443958"], "unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["840e017d-0142-4d0e-a80e-327ac44bc0c5"], "manufacturer_name": ["CVS Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL in 1 CARTON (51316-210-02)  / .1 mL in 1 VIAL (51316-210-01)", "package_ndc": "51316-210-02", "marketing_start_date": "20240424"}], "brand_name": "Naloxone Hydrochloride", "product_id": "51316-210_3c18b06c-be22-4076-84f8-80610dda1e61", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "51316-210", "generic_name": "Naloxone Hydrochloride", "labeler_name": "CVS Pharmacy, Inc", "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": "20240424", "listing_expiration_date": "20271231"}