Package 76420-132-01

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 76420-132-01
Digits Only 7642013201
Product NDC 76420-132
Product ID 76420-132_b2dde8d1-d0df-d7c2-e053-2995a90a2ed3
Description

100 g in 1 TUBE (76420-132-01)

Marketing

Marketing Status
Marketed Since 2020-10-30
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": "b2dde8d1-d0df-d7c2-e053-2995a90a2ed3", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["57d8513a-820a-46c5-b0c8-5aa1811b0e88"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 g in 1 TUBE (76420-132-01)", "package_ndc": "76420-132-01", "marketing_start_date": "20201030"}], "brand_name": "DICLOFENAC SODIUM", "product_id": "76420-132_b2dde8d1-d0df-d7c2-e053-2995a90a2ed3", "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": "76420-132", "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": "ANDA208301", "marketing_category": "ANDA", "marketing_start_date": "20160913", "listing_expiration_date": "20261231"}