Package 58602-609-07
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
58602-609-07
Digits Only
5860260907
Product NDC
58602-609
Description
1 TUBE in 1 CARTON (58602-609-07) / 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": "2a599579-b2b0-4423-8e30-fe04bf815870", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["2a599579-b2b0-4423-8e30-fe04bf815870"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (58602-609-07) / 100 g in 1 TUBE", "package_ndc": "58602-609-07", "marketing_start_date": "20230811"}], "brand_name": "Diclofenac Sodium", "product_id": "58602-609_2a599579-b2b0-4423-8e30-fe04bf815870", "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": "58602-609", "generic_name": "Diclofenac Sodium", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA204306", "marketing_category": "ANDA", "marketing_start_date": "20230811", "listing_expiration_date": "20261231"}