Package 63629-2077-1
Brand: diclofenac sodium delayed release
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
63629-2077-1
Digits Only
6362920771
Product NDC
63629-2077
Description
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-2077-1)
Marketing
Marketing Status
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": "3f8c444c-5789-4b85-a7c6-a215dbcc42ec", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["2b7462e6-62dc-4b08-9fbf-5858e356a7a8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-2077-1)", "package_ndc": "63629-2077-1", "marketing_start_date": "20210204"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "63629-2077_3f8c444c-5789-4b85-a7c6-a215dbcc42ec", "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": "63629-2077", "generic_name": "Diclofenac Sodium", "labeler_name": "Bryant Ranch Prepack", "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"}