Package 62032-414-20

Brand: tretinoin cream

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 62032-414-20
Digits Only 6203241420
Product NDC 62032-414
Description

1 TUBE in 1 CARTON (62032-414-20) / 20 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 1988-09-16
Brand tretinoin cream
Generic tretinoin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "c96be1f7-0c29-4bc7-ac51-c3da8b4788fb", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106302", "106303", "198300"], "spl_set_id": ["745cc3ce-60b4-4479-a055-316817567949"], "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": "1 TUBE in 1 CARTON (62032-414-20)  / 20 g in 1 TUBE", "package_ndc": "62032-414-20", "marketing_start_date": "19880916"}], "brand_name": "Tretinoin Cream", "product_id": "62032-414_c96be1f7-0c29-4bc7-ac51-c3da8b4788fb", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "62032-414", "generic_name": "tretinoin", "labeler_name": "Obagi Cosmeceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin Cream", "active_ingredients": [{"name": "TRETINOIN", "strength": ".25 mg/g"}], "application_number": "NDA019049", "marketing_category": "NDA", "marketing_start_date": "19880916", "listing_expiration_date": "20261231"}