Package 17089-382-18

Brand: guna-il 4

Generic: binetrakin
NDC Package

Package Facts

Identity

Package NDC 17089-382-18
Digits Only 1708938218
Product NDC 17089-382
Product ID 17089-382_ed819152-2968-22be-e053-2a95a90a33f6
Description

1 BOTTLE, DROPPER in 1 BOX (17089-382-18) / 30 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 2008-06-17
Brand guna-il 4
Generic binetrakin
Sample Package No

Linked Drug Pages (1)

GUNA-IL 4 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ed819152-2968-22be-e053-2a95a90a33f6", "openfda": {"upc": ["0317089382188"], "unii": ["751635Z921"], "spl_set_id": ["da1f5fe8-508d-4911-804a-8489ca97e071"], "manufacturer_name": ["Guna spa"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 BOX (17089-382-18)  / 30 mL in 1 BOTTLE, DROPPER", "package_ndc": "17089-382-18", "marketing_start_date": "20080617"}], "brand_name": "GUNA-IL 4", "product_id": "17089-382_ed819152-2968-22be-e053-2a95a90a33f6", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "17089-382", "generic_name": "BINETRAKIN", "labeler_name": "Guna spa", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GUNA-IL 4", "active_ingredients": [{"name": "BINETRAKIN", "strength": "4 [hp_C]/30mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20080617", "listing_expiration_date": "20261231"}