Package 50066-208-05

Brand: silka jock itch

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50066-208-05
Digits Only 5006620805
Product NDC 50066-208
Description

1 TUBE in 1 CARTON (50066-208-05) / 15 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2018-12-20
Brand silka jock itch
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "38f65202-ed21-e74d-e063-6294a90a2882", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["992528", "1739221"], "spl_set_id": ["326d8586-042f-44f8-8530-e46b7b777bc3"], "manufacturer_name": ["Genomma Lab USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (50066-208-05)  / 15 g in 1 TUBE", "package_ndc": "50066-208-05", "marketing_start_date": "20181220"}], "brand_name": "Silka Jock Itch", "product_id": "50066-208_38f65202-ed21-e74d-e063-6294a90a2882", "dosage_form": "CREAM", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "50066-208", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Genomma Lab USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Silka", "brand_name_suffix": "Jock Itch", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "ANDA077511", "marketing_category": "ANDA", "marketing_start_date": "20070702", "listing_expiration_date": "20261231"}