Package 68071-3826-2

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 68071-3826-2
Digits Only 6807138262
Product NDC 68071-3826
Description

1 TUBE in 1 CARTON (68071-3826-2) / 20 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-04-02
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": "31d2cd0d-3cb4-c719-e063-6294a90a2eb3", "openfda": {"nui": ["N0000175607", "M0018962"], "upc": ["0368071382624"], "unii": ["5688UTC01R"], "rxcui": ["198300"], "spl_set_id": ["31d2cd00-e534-6755-e063-6394a90ab8bb"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68071-3826-2)  / 20 g in 1 TUBE", "package_ndc": "68071-3826-2", "marketing_start_date": "20250402"}], "brand_name": "Tretinoin", "product_id": "68071-3826_31d2cd0d-3cb4-c719-e063-6294a90a2eb3", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "68071-3826", "generic_name": "tretinoin", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": "1 mg/g"}], "application_number": "ANDA211645", "marketing_category": "ANDA", "marketing_start_date": "20190122", "listing_expiration_date": "20261231"}