Package 71335-2925-1

Brand: podocon 25

Generic: podophyllum resin
NDC Package

Package Facts

Identity

Package NDC 71335-2925-1
Digits Only 7133529251
Product NDC 71335-2925
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (71335-2925-1) / 15 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2025-10-21
Brand podocon 25
Generic podophyllum resin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "c4e909ba-10b5-4c09-afea-4c5d151f657a", "openfda": {"unii": ["16902YVY2B"], "spl_set_id": ["790711b3-2168-4a19-b5c9-e46bf06143f6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (71335-2925-1)  / 15 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "71335-2925-1", "marketing_start_date": "20251021"}], "brand_name": "Podocon 25", "product_id": "71335-2925_c4e909ba-10b5-4c09-afea-4c5d151f657a", "dosage_form": "TINCTURE", "product_ndc": "71335-2925", "generic_name": "Podophyllum resin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Podocon 25", "active_ingredients": [{"name": "PODOPHYLLUM RESIN", "strength": "1 mg/4mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19900901", "listing_expiration_date": "20261231"}