Package 71610-068-80

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 71610-068-80
Digits Only 7161006880
Product NDC 71610-068
Product ID 71610-068_dc9b6499-7a34-4757-86b2-0880f3288048
Description

180 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-068-80)

Marketing

Marketing Status
Marketed Since 2018-05-14
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dc9b6499-7a34-4757-86b2-0880f3288048", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["e4af374a-1281-46af-a0a9-48820db6c947"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-068-80)", "package_ndc": "71610-068-80", "marketing_start_date": "20180514"}], "brand_name": "Diclofenac Sodium", "product_id": "71610-068_dc9b6499-7a34-4757-86b2-0880f3288048", "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": "71610-068", "generic_name": "Diclofenac Sodium", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA074514", "marketing_category": "ANDA", "marketing_start_date": "20150727", "listing_expiration_date": "20261231"}