Package 72162-1391-1
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
72162-1391-1
Digits Only
7216213911
Product NDC
72162-1391
Description
1 TUBE in 1 CARTON (72162-1391-1) / 100 g in 1 TUBE
Marketing
Marketing Status
Brand
diclofenac sodium
Generic
diclofenac sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "333b3bf8-b59e-4019-8bf9-8a781bce3c56", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["bf372e32-0902-447f-9673-00a3fcf0064c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (72162-1391-1) / 100 g in 1 TUBE", "package_ndc": "72162-1391-1", "marketing_start_date": "20181127"}], "brand_name": "diclofenac sodium", "product_id": "72162-1391_333b3bf8-b59e-4019-8bf9-8a781bce3c56", "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": "72162-1391", "generic_name": "diclofenac sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "diclofenac sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "30 mg/g"}], "application_number": "ANDA210893", "marketing_category": "ANDA", "marketing_start_date": "20181127", "listing_expiration_date": "20261231"}