Package 68788-8500-1

Brand: diclofenac sodium

Generic: diclofenac sodium topical gel, 1%
NDC Package

Package Facts

Identity

Package NDC 68788-8500-1
Digits Only 6878885001
Product NDC 68788-8500
Product ID 68788-8500_19c07b4b-87b2-4555-83e3-d7c49f67a08a
Description

1 TUBE in 1 CARTON (68788-8500-1) / 100 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2023-08-11
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": "19c07b4b-87b2-4555-83e3-d7c49f67a08a", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["361dc5f9-aa20-42a5-b0d5-d8c732751915"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68788-8500-1)  / 100 g in 1 TUBE", "package_ndc": "68788-8500-1", "marketing_start_date": "20230811"}], "brand_name": "DICLOFENAC SODIUM", "product_id": "68788-8500_19c07b4b-87b2-4555-83e3-d7c49f67a08a", "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": "68788-8500", "generic_name": "diclofenac sodium topical gel, 1%", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DICLOFENAC SODIUM", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA210986", "marketing_category": "ANDA", "marketing_start_date": "20230811", "listing_expiration_date": "20261231"}