Package 68788-7270-1
Brand: diclofenac sodium
Generic: diclofenacPackage Facts
Identity
Package NDC
68788-7270-1
Digits Only
6878872701
Product NDC
68788-7270
Description
1 BOTTLE in 1 CARTON (68788-7270-1) / 150 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
diclofenac sodium
Generic
diclofenac
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "ff81467f-1bc6-433c-9119-a4e9b1ab0011", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["937e9ba5-cdad-4e72-a77a-bad699e1b236"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68788-7270-1) / 150 mL in 1 BOTTLE", "package_ndc": "68788-7270-1", "marketing_start_date": "20190111"}], "brand_name": "Diclofenac Sodium", "product_id": "68788-7270_ff81467f-1bc6-433c-9119-a4e9b1ab0011", "dosage_form": "SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-7270", "generic_name": "Diclofenac", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA206116", "marketing_category": "ANDA", "marketing_start_date": "20190111", "listing_expiration_date": "20261231"}