Package 71335-2915-1

Brand: ciclopirox olamine

Generic: ciclopirox olamine
NDC Package

Package Facts

Identity

Package NDC 71335-2915-1
Digits Only 7133529151
Product NDC 71335-2915
Product ID 71335-2915_60371a57-545f-458b-8ca1-016eb9b78629
Description

1 BOTTLE in 1 CARTON (71335-2915-1) / 30 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-10-24
Brand ciclopirox olamine
Generic ciclopirox olamine
Sample Package No

Linked Drug Pages (1)

Ciclopirox Olamine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "60371a57-545f-458b-8ca1-016eb9b78629", "openfda": {"unii": ["50MD4SB4AP"], "rxcui": ["309290"], "spl_set_id": ["835a6370-f331-4b15-b6fa-beafe027f187"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71335-2915-1)  / 30 mL in 1 BOTTLE", "package_ndc": "71335-2915-1", "marketing_start_date": "20251024"}], "brand_name": "Ciclopirox Olamine", "product_id": "71335-2915_60371a57-545f-458b-8ca1-016eb9b78629", "dosage_form": "SUSPENSION", "pharm_class": ["Decreased DNA Replication [PE]", "Decreased Protein Synthesis [PE]", "Decreased RNA Replication [PE]", "Protein Synthesis Inhibitors [MoA]"], "product_ndc": "71335-2915", "generic_name": "Ciclopirox Olamine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciclopirox Olamine", "active_ingredients": [{"name": "CICLOPIROX OLAMINE", "strength": "7.7 mg/100mL"}], "application_number": "ANDA077676", "marketing_category": "ANDA", "marketing_start_date": "20061229", "listing_expiration_date": "20261231"}