Package 12539-146-02

Brand: nafasolina

Generic: naphazoline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 12539-146-02
Digits Only 1253914602
Product NDC 12539-146
Description

1 BOTTLE, DROPPER in 1 CARTON (12539-146-02) / 14.7868 mL in 1 BOTTLE, DROPPER (12539-146-01)

Marketing

Marketing Status
Marketed Since 2025-03-20
Brand nafasolina
Generic naphazoline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "463c40c9-6e49-e804-e063-6394a90a3db8", "openfda": {"unii": ["MZ1131787D"], "rxcui": ["1046602"], "spl_set_id": ["30cade3d-208f-8594-e063-6394a90ad2a0"], "manufacturer_name": ["Doral Pharmamedics Inc DBA AG Marin Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (12539-146-02)  / 14.7868 mL in 1 BOTTLE, DROPPER (12539-146-01)", "package_ndc": "12539-146-02", "marketing_start_date": "20250320"}], "brand_name": "NAFASOLINA", "product_id": "12539-146_463c40c9-6e49-e804-e063-6394a90a3db8", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "12539-146", "generic_name": "Naphazoline hydrochloride", "labeler_name": "Doral Pharmamedics Inc DBA AG Marin Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NAFASOLINA", "active_ingredients": [{"name": "NAPHAZOLINE HYDROCHLORIDE", "strength": "50 mg/100mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250320", "listing_expiration_date": "20261231"}