Package 51655-280-52

Brand: diclofenac sodium delayed release

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 51655-280-52
Digits Only 5165528052
Product NDC 51655-280
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-280-52)

Marketing

Marketing Status
Marketed Since 2022-10-26
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": "48e702c3-71aa-a566-e063-6394a90a7778", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["f2b7ea75-738b-54a8-e053-2995a90a00d5"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-280-26)", "package_ndc": "51655-280-26", "marketing_start_date": "20221206"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-280-52)", "package_ndc": "51655-280-52", "marketing_start_date": "20221026"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "51655-280_48e702c3-71aa-a566-e063-6394a90a7778", "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": "51655-280", "generic_name": "Diclofenac Sodium", "labeler_name": "Northwind Health Company, LLC", "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": "20221026", "listing_expiration_date": "20271231"}