Package 83324-301-01

Brand: maximum strength antifungal liquid

Generic: tolnaftate
NDC Package

Package Facts

Identity

Package NDC 83324-301-01
Digits Only 8332430101
Product NDC 83324-301
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (83324-301-01) / 30 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2024-06-07
Brand maximum strength antifungal liquid
Generic tolnaftate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "42f3ee4e-216c-fc82-e063-6394a90a2a06", "openfda": {"unii": ["06KB629TKV"], "rxcui": ["313423"], "spl_set_id": ["1a4f4d10-6782-ddb4-e063-6294a90ac206"], "manufacturer_name": ["Chain Drug Marketing Association Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (83324-301-01)  / 30 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "83324-301-01", "marketing_start_date": "20240607"}], "brand_name": "Maximum Strength Antifungal Liquid", "product_id": "83324-301_42f3ee4e-216c-fc82-e063-6394a90a2a06", "dosage_form": "LIQUID", "product_ndc": "83324-301", "generic_name": "Tolnaftate", "labeler_name": "Chain Drug Marketing Association Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Antifungal Liquid", "active_ingredients": [{"name": "TOLNAFTATE", "strength": "10 mg/mL"}], "application_number": "M005", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240607", "listing_expiration_date": "20261231"}