Package 72162-2518-6

Brand: diclofenac sodium misoprostol

Generic: diclofenac sodium and misoprostol
NDC Package

Package Facts

Identity

Package NDC 72162-2518-6
Digits Only 7216225186
Product NDC 72162-2518
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2518-6)

Marketing

Marketing Status
Marketed Since 2025-06-13
Brand diclofenac sodium misoprostol
Generic diclofenac sodium and misoprostol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "377c0f85-1a9b-fd44-e063-6394a90a8e1e", "openfda": {"nui": ["N0000175785", "M0017811"], "unii": ["QTG126297Q", "0E43V0BB57"], "rxcui": ["857706"], "spl_set_id": ["de4c02a5-87e8-42f5-a9ff-f409ff9e6d62"], "pharm_class_cs": ["Prostaglandins E, Synthetic [CS]"], "pharm_class_epc": ["Prostaglandin E1 Analog [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2518-6)", "package_ndc": "72162-2518-6", "marketing_start_date": "20250613"}], "brand_name": "Diclofenac Sodium Misoprostol", "product_id": "72162-2518_377c0f85-1a9b-fd44-e063-6394a90a8e1e", "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]", "Prostaglandin E1 Analog [EPC]", "Prostaglandins E", "Synthetic [CS]"], "product_ndc": "72162-2518", "generic_name": "diclofenac sodium and misoprostol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium Misoprostol", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}, {"name": "MISOPROSTOL", "strength": "200 ug/1"}], "application_number": "ANDA205143", "marketing_category": "ANDA", "marketing_start_date": "20210715", "listing_expiration_date": "20261231"}