Package 72162-2158-2

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 72162-2158-2
Digits Only 7216221582
Product NDC 72162-2158
Description

1 TUBE in 1 CARTON (72162-2158-2) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2023-12-07
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": "7acc082c-03e7-48b6-b320-e9a48401356b", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106303"], "spl_set_id": ["8929196c-389a-4c43-843c-00fbb26a1dd9"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (72162-2158-2)  / 45 g in 1 TUBE", "package_ndc": "72162-2158-2", "marketing_start_date": "20231207"}], "brand_name": "TRETINOIN", "product_id": "72162-2158_7acc082c-03e7-48b6-b320-e9a48401356b", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "72162-2158", "generic_name": "tretinoin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRETINOIN", "active_ingredients": [{"name": "TRETINOIN", "strength": ".5 mg/g"}], "application_number": "ANDA075265", "marketing_category": "ANDA", "marketing_start_date": "20170426", "listing_expiration_date": "20261231"}