Package 76420-025-01

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 76420-025-01
Digits Only 7642002501
Product NDC 76420-025
Product ID 76420-025_a843b00f-4da3-1901-e053-2a95a90affae
Description

100 g in 1 TUBE (76420-025-01)

Marketing

Marketing Status
Marketed Since 2020-06-17
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": "a843b00f-4da3-1901-e053-2a95a90affae", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["1e39f8d4-56a2-4d29-a971-495574e8d4a7"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 g in 1 TUBE (76420-025-01)", "package_ndc": "76420-025-01", "marketing_start_date": "20200617"}], "brand_name": "Diclofenac Sodium", "product_id": "76420-025_a843b00f-4da3-1901-e053-2a95a90affae", "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": "76420-025", "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": "ANDA200936", "marketing_category": "ANDA", "marketing_start_date": "20131121", "listing_expiration_date": "20261231"}