Package 68788-7772-1

Brand: diclofenac sodium

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

Package Facts

Identity

Package NDC 68788-7772-1
Digits Only 6878877721
Product NDC 68788-7772
Product ID 68788-7772_f86c3fa2-c940-4d96-9468-d4966d4aad20
Description

1 TUBE in 1 CARTON (68788-7772-1) / 100 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2020-08-03
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": "f86c3fa2-c940-4d96-9468-d4966d4aad20", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["aee20924-79ab-400e-b9b6-418978914654"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68788-7772-1)  / 100 g in 1 TUBE", "package_ndc": "68788-7772-1", "marketing_start_date": "20200803"}], "brand_name": "Diclofenac Sodium", "product_id": "68788-7772_f86c3fa2-c940-4d96-9468-d4966d4aad20", "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": "68788-7772", "generic_name": "Diclofenac Sodium Topical Gel, 1%,", "labeler_name": "Preferred Pharmaceuticals, 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": "20200803", "listing_expiration_date": "20261231"}