Package 72189-479-01

Brand: diclofenac sodium gel

Generic: diclofenac sodium gel
NDC Package

Package Facts

Identity

Package NDC 72189-479-01
Digits Only 7218947901
Product NDC 72189-479
Product ID 72189-479_2c4e167d-2908-0703-e063-6394a90a9132
Description

1 g in 1 TUBE (72189-479-01)

Marketing

Marketing Status
Marketed Since 2023-05-30
Brand diclofenac sodium gel
Generic diclofenac sodium gel
Sample Package No

Linked Drug Pages (1)

Diclofenac Sodium Gel ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2c4e167d-2908-0703-e063-6394a90a9132", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["fce9b3eb-ae79-a090-e053-6294a90ad20e"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "1 g in 1 TUBE (72189-479-01)", "package_ndc": "72189-479-01", "marketing_start_date": "20230530"}], "brand_name": "Diclofenac Sodium Gel", "product_id": "72189-479_2c4e167d-2908-0703-e063-6394a90a9132", "dosage_form": "GEL", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72189-479", "generic_name": "Diclofenac Sodium Gel", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium Gel", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA210986", "marketing_category": "ANDA", "marketing_start_date": "20230530", "listing_expiration_date": "20261231"}