Package 68788-4069-2

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 68788-4069-2
Digits Only 6878840692
Product NDC 68788-4069
Product ID 68788-4069_d6819051-4748-479e-8b53-c298edcbd410
Description

1 TUBE in 1 CARTON (68788-4069-2) / 20 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2026-01-28
Brand tretinoin
Generic tretinoin
Sample Package No

Linked Drug Pages (1)

TRETINOIN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "d6819051-4748-479e-8b53-c298edcbd410", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106302"], "spl_set_id": ["d6819051-4748-479e-8b53-c298edcbd410"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68788-4069-2)  / 20 g in 1 TUBE", "package_ndc": "68788-4069-2", "marketing_start_date": "20260128"}], "brand_name": "TRETINOIN", "product_id": "68788-4069_d6819051-4748-479e-8b53-c298edcbd410", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "68788-4069", "generic_name": "tretinoin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRETINOIN", "active_ingredients": [{"name": "TRETINOIN", "strength": ".25 mg/g"}], "application_number": "ANDA075264", "marketing_category": "ANDA", "marketing_start_date": "20260128", "listing_expiration_date": "20271231"}