Package 35356-714-60

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 35356-714-60
Digits Only 3535671460
Product NDC 35356-714
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (35356-714-60)

Marketing

Marketing Status
Discontinued 2026-07-31
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7c056476-691c-45b0-91dd-3086105c1122", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906", "855926"], "spl_set_id": ["bfa8cb40-3528-4d41-ae77-444e521e30c0"], "manufacturer_name": ["Quality Care Products LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (35356-714-60)", "package_ndc": "35356-714-60", "marketing_end_date": "20260731", "marketing_start_date": "20130207"}], "brand_name": "Diclofenac Sodium", "product_id": "35356-714_7c056476-691c-45b0-91dd-3086105c1122", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "35356-714", "generic_name": "Diclofenac Sodium", "labeler_name": "Quality Care Products LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA077863", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20080819"}