Package 68788-9435-1

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 68788-9435-1
Digits Only 6878894351
Product NDC 68788-9435
Product ID 68788-9435_7909ce18-1906-4d64-b330-81c1c4c5ec88
Description

1 TUBE in 1 CARTON (68788-9435-1) / 100 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2018-06-08
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": "7909ce18-1906-4d64-b330-81c1c4c5ec88", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["5d0a4b41-afbf-45e7-bb1c-587d72314ee0"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68788-9435-1)  / 100 g in 1 TUBE", "package_ndc": "68788-9435-1", "marketing_start_date": "20180608"}], "brand_name": "DICLOFENAC SODIUM", "product_id": "68788-9435_7909ce18-1906-4d64-b330-81c1c4c5ec88", "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": "68788-9435", "generic_name": "diclofenac sodium", "labeler_name": "Preferred Pharmaceuticals 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": "20180608", "listing_expiration_date": "20261231"}