Package 0781-7172-50

Brand: azelaic acid gel

Generic: azelaic acid
NDC Package

Package Facts

Identity

Package NDC 0781-7172-50
Digits Only 0781717250
Product NDC 0781-7172
Description

1 TUBE in 1 CARTON (0781-7172-50) / 50 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2018-10-01
Brand azelaic acid gel
Generic azelaic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d6c8343f-d169-4924-9fa2-4fbf097a32a7", "openfda": {"nui": ["N0000008841", "N0000009982"], "unii": ["F2VW3D43YT"], "rxcui": ["1041518"], "spl_set_id": ["66178511-5c1a-4ecd-bc98-2ceb54e710ac"], "pharm_class_pe": ["Decreased Protein Synthesis [PE]", "Decreased Sebaceous Gland Activity [PE]"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0781-7172-50)  / 50 g in 1 TUBE", "package_ndc": "0781-7172-50", "marketing_start_date": "20181001"}], "brand_name": "Azelaic Acid Gel", "product_id": "0781-7172_d6c8343f-d169-4924-9fa2-4fbf097a32a7", "dosage_form": "GEL", "pharm_class": ["Decreased Protein Synthesis [PE]", "Decreased Sebaceous Gland Activity [PE]"], "product_ndc": "0781-7172", "generic_name": "azelaic acid", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azelaic Acid Gel", "active_ingredients": [{"name": "AZELAIC ACID", "strength": ".15 g/g"}], "application_number": "NDA021470", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20181001", "listing_expiration_date": "20261231"}