Package 63629-3726-1

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 63629-3726-1
Digits Only 6362937261
Product NDC 63629-3726
Product ID 63629-3726_10240c13-0057-4ffe-ad17-12d20613bdb6
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-3726-1)

Marketing

Marketing Status
Marketed Since 2024-04-02
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Diclofenac Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10240c13-0057-4ffe-ad17-12d20613bdb6", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855664"], "spl_set_id": ["4e97c685-628a-4b83-ba9e-2d3caf65542b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-3726-1)", "package_ndc": "63629-3726-1", "marketing_start_date": "20240402"}], "brand_name": "Diclofenac Sodium", "product_id": "63629-3726_10240c13-0057-4ffe-ad17-12d20613bdb6", "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": "63629-3726", "generic_name": "Diclofenac Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "25 mg/1"}], "application_number": "ANDA090066", "marketing_category": "ANDA", "marketing_start_date": "20101231", "listing_expiration_date": "20261231"}