Package 0591-2971-99

Brand: Naloxone Hydrochloride

Generic: Naloxone Hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0591-2971-99
Digits Only 0591297199
Product NDC 0591-2971
Product ID 0591-2971_1ef1e344-e325-46f4-9dbd-1bec7ccf34dd
Description

2 BLISTER PACK in 1 CARTON (0591-2971-99) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (0591-2971-54) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Discontinued 2026-02-28
Brand Naloxone Hydrochloride
Generic Naloxone Hydrochloride
Sample Package No

Linked Drug Pages (1)

Naloxone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "1ef1e344-e325-46f4-9dbd-1bec7ccf34dd", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["e7f81903-ee0d-4909-8e06-f58c9e56a6fc"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0591-2971-99)  / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (0591-2971-54)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0591-2971-99", "marketing_end_date": "20260228", "marketing_start_date": "20230120"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0591-2971_1ef1e344-e325-46f4-9dbd-1bec7ccf34dd", "dosage_form": "SPRAY, METERED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0591-2971", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "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": "20260228", "marketing_start_date": "20230120"}