Package 42192-714-01

Brand: ciclopirox

Generic: ciclopirox
NDC Package

Package Facts

Identity

Package NDC 42192-714-01
Digits Only 4219271401
Product NDC 42192-714
Product ID 42192-714_0fa6cf7e-6dc3-44a9-b1d1-f30e4feb367c
Description

1 KIT in 1 CARTON (42192-714-01) * 6.6 mL in 1 BOTTLE, WITH APPLICATOR * 28 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2011-10-10
Brand ciclopirox
Generic ciclopirox
Sample Package No

Linked Drug Pages (1)

Ciclopirox ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "0fa6cf7e-6dc3-44a9-b1d1-f30e4feb367c", "openfda": {"rxcui": ["309291"], "spl_set_id": ["2c67dd09-ab1f-4ccf-97b5-421356f64f22"], "manufacturer_name": ["Acella Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (42192-714-01)  *  6.6 mL in 1 BOTTLE, WITH APPLICATOR *  28 mL in 1 BOTTLE", "package_ndc": "42192-714-01", "marketing_start_date": "20111010"}], "brand_name": "Ciclopirox", "product_id": "42192-714_0fa6cf7e-6dc3-44a9-b1d1-f30e4feb367c", "dosage_form": "KIT", "product_ndc": "42192-714", "generic_name": "Ciclopirox", "labeler_name": "Acella Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciclopirox", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20111010", "listing_expiration_date": "20261231"}