Package 76420-091-01

Brand: diclofenac sodium

Generic: diclofenac sodium topical gel, 1%,
NDC Package

Package Facts

Identity

Package NDC 76420-091-01
Digits Only 7642009101
Product NDC 76420-091
Product ID 76420-091_b269742f-932d-73f2-e053-2a95a90a3761
Description

100 g in 1 TUBE (76420-091-01)

Marketing

Marketing Status
Marketed Since 2020-10-24
Brand diclofenac sodium
Generic diclofenac sodium topical gel, 1%,
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": "b269742f-932d-73f2-e053-2a95a90a3761", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["988abe66-0b3b-4c13-87b4-adc913227fc5"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 g in 1 TUBE (76420-091-01)", "package_ndc": "76420-091-01", "marketing_start_date": "20201024"}], "brand_name": "Diclofenac Sodium", "product_id": "76420-091_b269742f-932d-73f2-e053-2a95a90a3761", "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": "76420-091", "generic_name": "Diclofenac Sodium Topical Gel, 1%,", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA210986", "marketing_category": "ANDA", "marketing_start_date": "20200130", "listing_expiration_date": "20261231"}