Package 80425-0210-1

Brand: diclofenac sodium er

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 80425-0210-1
Digits Only 8042502101
Product NDC 80425-0210
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (80425-0210-1)

Marketing

Marketing Status
Marketed Since 2023-11-04
Brand diclofenac sodium er
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a99b834-0c9e-6f97-e063-6394a90a8407", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["ecaa39b8-067c-80d7-e053-2a95a90a7354"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (80425-0210-1)", "package_ndc": "80425-0210-1", "marketing_start_date": "20231104"}], "brand_name": "Diclofenac Sodium ER", "product_id": "80425-0210_2a99b834-0c9e-6f97-e063-6394a90a8407", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0210", "generic_name": "Diclofenac Sodium", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "ER", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA075492", "marketing_category": "ANDA", "marketing_start_date": "20221104", "listing_expiration_date": "20261231"}