Package 50090-4172-1

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 50090-4172-1
Digits Only 5009041721
Product NDC 50090-4172
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4172-1)

Marketing

Marketing Status
Marketed Since 2019-03-07
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9c9c3f13-4e0f-4f4a-8065-6bd89a25ff96", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["d9698809-4887-4514-aa28-0066355ef908"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4172-1)", "package_ndc": "50090-4172-1", "marketing_start_date": "20190307"}], "brand_name": "Diclofenac Sodium", "product_id": "50090-4172_9c9c3f13-4e0f-4f4a-8065-6bd89a25ff96", "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": "50090-4172", "generic_name": "Diclofenac Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA075492", "marketing_category": "ANDA", "marketing_start_date": "20000228", "listing_expiration_date": "20261231"}