Package 76420-261-01

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 76420-261-01
Digits Only 7642026101
Product NDC 76420-261
Product ID 76420-261_e709b84d-fa7d-3f23-e053-2995a90aacd3
Description

1 TUBE in 1 CARTON (76420-261-01) / 100 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2022-08-24
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Diclofenac Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "e709b84d-fa7d-3f23-e053-2995a90aacd3", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["b162d65d-b105-4a68-90bb-316b9686267b"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (76420-261-01)  / 100 g in 1 TUBE", "package_ndc": "76420-261-01", "marketing_start_date": "20220824"}], "brand_name": "Diclofenac Sodium", "product_id": "76420-261_e709b84d-fa7d-3f23-e053-2995a90aacd3", "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": "76420-261", "generic_name": "Diclofenac Sodium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "30 mg/g"}], "application_number": "ANDA206493", "marketing_category": "ANDA", "marketing_start_date": "20160519", "listing_expiration_date": "20261231"}