Package 50090-7171-0

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 50090-7171-0
Digits Only 5009071710
Product NDC 50090-7171
Product ID 50090-7171_e078fd97-82cd-43fb-b32b-4ff103a76f92
Description

1 TUBE in 1 CARTON (50090-7171-0) / 20 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-05-20
Brand tretinoin
Generic tretinoin
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "e078fd97-82cd-43fb-b32b-4ff103a76f92", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106302"], "spl_set_id": ["06ebaf8e-3648-493e-9b6a-9adef67bc65f"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (50090-7171-0)  / 20 g in 1 TUBE", "package_ndc": "50090-7171-0", "marketing_start_date": "20240520"}], "brand_name": "Tretinoin", "product_id": "50090-7171_e078fd97-82cd-43fb-b32b-4ff103a76f92", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "50090-7171", "generic_name": "tretinoin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".25 mg/g"}], "application_number": "ANDA215713", "marketing_category": "ANDA", "marketing_start_date": "20230105", "listing_expiration_date": "20261231"}