Package 70518-3233-0

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 70518-3233-0
Digits Only 7051832330
Product NDC 70518-3233
Product ID 70518-3233_3a35c95b-10e9-689f-e063-6394a90ae1d4
Description

1 TUBE in 1 CARTON (70518-3233-0) / 20 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2021-10-11
Brand tretinoin
Generic tretinoin
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3a35c95b-10e9-689f-e063-6394a90ae1d4", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["198300"], "spl_set_id": ["c4d5155b-046d-4f94-bafc-651b572c2bd5"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70518-3233-0)  / 20 g in 1 TUBE", "package_ndc": "70518-3233-0", "marketing_start_date": "20211011"}], "brand_name": "TRETINOIN", "product_id": "70518-3233_3a35c95b-10e9-689f-e063-6394a90ae1d4", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "70518-3233", "generic_name": "tretinoin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRETINOIN", "active_ingredients": [{"name": "TRETINOIN", "strength": "1 mg/g"}], "application_number": "ANDA075213", "marketing_category": "ANDA", "marketing_start_date": "20211011", "listing_expiration_date": "20261231"}