Package 68071-3184-6

Brand: diclofenac sodium delayed release

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3184-6
Digits Only 6807131846
Product NDC 68071-3184
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-6)

Marketing

Marketing Status
Marketed Since 2017-03-21
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": "1da0c34e-cc8a-9db7-e063-6394a90afe92", "openfda": {"upc": ["0368071318463"], "unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["4b44ac98-225c-1739-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-1)", "package_ndc": "68071-3184-1", "marketing_start_date": "20170321"}, {"sample": false, "description": "20 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-2)", "package_ndc": "68071-3184-2", "marketing_start_date": "20170321"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-3)", "package_ndc": "68071-3184-3", "marketing_start_date": "20170321"}, {"sample": false, "description": "45 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-5)", "package_ndc": "68071-3184-5", "marketing_start_date": "20170321"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-6)", "package_ndc": "68071-3184-6", "marketing_start_date": "20170321"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-9)", "package_ndc": "68071-3184-9", "marketing_start_date": "20170321"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "68071-3184_1da0c34e-cc8a-9db7-e063-6394a90afe92", "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": "68071-3184", "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": "50 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "19981113", "listing_expiration_date": "20261231"}