Package 51655-230-52

Brand: diclofenac potassium

Generic: diclofenac potassium
NDC Package

Package Facts

Identity

Package NDC 51655-230-52
Digits Only 5165523052
Product NDC 51655-230
Description

30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-230-52)

Marketing

Marketing Status
Marketed Since 2022-10-27
Brand diclofenac potassium
Generic diclofenac potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d2c42f-dd1c-d0e8-e063-6294a90a76f7", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["f2b6a4dd-e4e2-4acc-e053-2995a90aebf2"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-230-52)", "package_ndc": "51655-230-52", "marketing_start_date": "20221027"}], "brand_name": "Diclofenac Potassium", "product_id": "51655-230_48d2c42f-dd1c-d0e8-e063-6294a90a76f7", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51655-230", "generic_name": "diclofenac potassium", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA075229", "marketing_category": "ANDA", "marketing_start_date": "20221027", "listing_expiration_date": "20271231"}