Package 68071-4117-9

Brand: diclofenac sodium delayed release

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 68071-4117-9
Digits Only 6807141179
Product NDC 68071-4117
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-9)

Marketing

Marketing Status
Marketed Since 2017-10-11
Brand diclofenac sodium delayed release
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ac051d3-1a25-8e90-e063-6294a90a7baa", "openfda": {"upc": ["0368071411720"], "unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["5b4c1a15-ed93-7192-e053-2991aa0a8360"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-2)", "package_ndc": "68071-4117-2", "marketing_start_date": "20171011"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-3)", "package_ndc": "68071-4117-3", "marketing_start_date": "20171011"}, {"sample": false, "description": "14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-4)", "package_ndc": "68071-4117-4", "marketing_start_date": "20171011"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-6)", "package_ndc": "68071-4117-6", "marketing_start_date": "20171011"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-9)", "package_ndc": "68071-4117-9", "marketing_start_date": "20171011"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "68071-4117_2ac051d3-1a25-8e90-e063-6294a90a7baa", "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": "68071-4117", "generic_name": "Diclofenac Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "19981113", "listing_expiration_date": "20261231"}