Package 72162-2303-2

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 72162-2303-2
Digits Only 7216223032
Product NDC 72162-2303
Description

1 BOTTLE, PUMP in 1 CARTON (72162-2303-2) / 50 g in 1 BOTTLE, PUMP

Marketing

Marketing Status
Marketed Since 2024-04-30
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": "d4a78cfd-7499-4e65-9c01-e97fa7545caa", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["1488045"], "spl_set_id": ["2b58cf56-e713-4cdd-8b4e-e6651ef76650"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PUMP in 1 CARTON (72162-2303-2)  / 50 g in 1 BOTTLE, PUMP", "package_ndc": "72162-2303-2", "marketing_start_date": "20240430"}], "brand_name": "Tretinoin", "product_id": "72162-2303_d4a78cfd-7499-4e65-9c01-e97fa7545caa", "dosage_form": "GEL", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "72162-2303", "generic_name": "Tretinoin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".8 mg/g"}], "application_number": "ANDA215609", "marketing_category": "ANDA", "marketing_start_date": "20230824", "listing_expiration_date": "20271231"}