Package 0472-1783-10

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 0472-1783-10
Digits Only 0472178310
Product NDC 0472-1783
Description

1 TUBE in 1 CARTON (0472-1783-10) / 100 g in 1 TUBE

Marketing

Marketing Status
Discontinued 2027-02-28
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": "6b4784a2-31ca-485a-9bff-6c322c0cb902", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["74169b2d-ac56-4757-86c4-cdcfcd5f4eb5"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0472-1783-10)  / 100 g in 1 TUBE", "package_ndc": "0472-1783-10", "marketing_end_date": "20270228", "marketing_start_date": "20160519"}], "brand_name": "Diclofenac Sodium", "product_id": "0472-1783_6b4784a2-31ca-485a-9bff-6c322c0cb902", "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": "0472-1783", "generic_name": "Diclofenac Sodium", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "30 mg/g"}], "application_number": "ANDA206493", "marketing_category": "ANDA", "marketing_end_date": "20270228", "marketing_start_date": "20160519"}