Package 72189-379-01

Brand: diclofenac sodium gel

Generic: diclofenac sodium gel
NDC Package

Package Facts

Identity

Package NDC 72189-379-01
Digits Only 7218937901
Product NDC 72189-379
Product ID 72189-379_2c4ccc7d-5cb0-43b5-e063-6294a90a05ec
Description

1 g in 1 TUBE (72189-379-01)

Marketing

Marketing Status
Marketed Since 2022-09-08
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": "2c4ccc7d-5cb0-43b5-e063-6294a90a05ec", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["e82e4d34-bdaa-b950-e053-2995a90a29f1"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "1 g in 1 TUBE (72189-379-01)", "package_ndc": "72189-379-01", "marketing_start_date": "20220908"}], "brand_name": "Diclofenac Sodium Gel", "product_id": "72189-379_2c4ccc7d-5cb0-43b5-e063-6294a90a05ec", "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": "72189-379", "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": "30 mg/g"}], "application_number": "ANDA208301", "marketing_category": "ANDA", "marketing_start_date": "20220908", "listing_expiration_date": "20261231"}