Package 71335-2898-1

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 71335-2898-1
Digits Only 7133528981
Product NDC 71335-2898
Product ID 71335-2898_ca82745d-d880-4b6a-af76-97b8ce1519ab
Description

1 TUBE in 1 CARTON (71335-2898-1) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-10-21
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": "ca82745d-d880-4b6a-af76-97b8ce1519ab", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["313451"], "spl_set_id": ["a1ae0000-3411-47e5-94f2-ae2ee70eadfb"], "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 (71335-2898-1)  / 45 g in 1 TUBE", "package_ndc": "71335-2898-1", "marketing_start_date": "20251021"}], "brand_name": "Tretinoin", "product_id": "71335-2898_ca82745d-d880-4b6a-af76-97b8ce1519ab", "dosage_form": "GEL", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "71335-2898", "generic_name": "Tretinoin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".25 mg/g"}], "application_number": "NDA017579", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190712", "listing_expiration_date": "20261231"}