Package 68788-8952-6

Brand: diclofenac sodium delayed release

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 68788-8952-6
Digits Only 6878889526
Product NDC 68788-8952
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-6)

Marketing

Marketing Status
Marketed Since 2015-11-20
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": "bef4d22d-6e29-46ed-bb04-55b1b18e7f20", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["e947653c-6789-4c15-82c9-4b1402f6d6ac"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-1)", "package_ndc": "68788-8952-1", "marketing_start_date": "20151120"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-3)", "package_ndc": "68788-8952-3", "marketing_start_date": "20151120"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-6)", "package_ndc": "68788-8952-6", "marketing_start_date": "20151120"}, {"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-8)", "package_ndc": "68788-8952-8", "marketing_start_date": "20151120"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-9)", "package_ndc": "68788-8952-9", "marketing_start_date": "20151120"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "68788-8952_bef4d22d-6e29-46ed-bb04-55b1b18e7f20", "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": "68788-8952", "generic_name": "Diclofenac Sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "20151120", "listing_expiration_date": "20261231"}