Package 62032-413-20

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 62032-413-20
Digits Only 6203241320
Product NDC 62032-413
Description

20 g in 1 TUBE (62032-413-20)

Marketing

Marketing Status
Marketed Since 2014-06-19
Brand tretinoin
Generic tretinoin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "cf3898ce-f8a0-4e8f-a237-a8d87e3c20a3", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["245723"], "spl_set_id": ["c5ee36ac-2ffd-4cca-ad47-b1dae7ebdb3b"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Obagi Cosmeceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 g in 1 TUBE (62032-413-20)", "package_ndc": "62032-413-20", "marketing_start_date": "20140619"}], "brand_name": "Tretinoin", "product_id": "62032-413_cf3898ce-f8a0-4e8f-a237-a8d87e3c20a3", "dosage_form": "GEL", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "62032-413", "generic_name": "Tretinoin", "labeler_name": "Obagi Cosmeceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".05 g/100g"}], "application_number": "NDA022070", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20140619", "listing_expiration_date": "20261231"}