Package 71335-2952-1

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 71335-2952-1
Digits Only 7133529521
Product NDC 71335-2952
Product ID 71335-2952_8f5850a4-4294-418c-8b1f-65f229e5973f
Description

1 TUBE in 1 CARTON (71335-2952-1) / 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": "8f5850a4-4294-418c-8b1f-65f229e5973f", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["313450"], "spl_set_id": ["04f14d6e-5b44-44bd-a7f3-d684d9c5d7cb"], "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 (71335-2952-1)  / 45 g in 1 TUBE", "package_ndc": "71335-2952-1", "marketing_start_date": "20251021"}], "brand_name": "Tretinoin", "product_id": "71335-2952_8f5850a4-4294-418c-8b1f-65f229e5973f", "dosage_form": "GEL", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "71335-2952", "generic_name": "Tretinoin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".1 mg/g"}], "application_number": "NDA017955", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190812", "listing_expiration_date": "20261231"}