Package 50090-3316-0

Brand: diclofenac sodium

Generic: diclofenac
NDC Package

Package Facts

Identity

Package NDC 50090-3316-0
Digits Only 5009033160
Product NDC 50090-3316
Description

1 BOTTLE in 1 CARTON (50090-3316-0) / 150 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-12-28
Brand diclofenac sodium
Generic diclofenac
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "49ad4cc4-ab83-4966-b18b-20b43b9120e8", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["857700"], "spl_set_id": ["58178f0d-3960-48e3-91ba-150f691be241"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50090-3316-0)  / 150 mL in 1 BOTTLE", "package_ndc": "50090-3316-0", "marketing_start_date": "20171228"}], "brand_name": "Diclofenac Sodium", "product_id": "50090-3316_49ad4cc4-ab83-4966-b18b-20b43b9120e8", "dosage_form": "SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-3316", "generic_name": "Diclofenac", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "16.05 mg/mL"}], "application_number": "ANDA206116", "marketing_category": "ANDA", "marketing_start_date": "20160902", "listing_expiration_date": "20261231"}