Package 69306-750-03

Brand: diclofenac potassium

Generic: diclofenac potassium
NDC Package

Package Facts

Identity

Package NDC 69306-750-03
Digits Only 6930675003
Product NDC 69306-750
Product ID 69306-750_42fd182d-4a2e-7058-e063-6294a90a63f9
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69306-750-03)

Marketing

Marketing Status
Marketed Since 2025-11-07
Brand diclofenac potassium
Generic diclofenac potassium
Sample Package No

Linked Drug Pages (1)

Diclofenac Potassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42fd182d-4a2e-7058-e063-6294a90a63f9", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["6394ab5f-b3ff-4397-97eb-ff92485c5ec0"], "manufacturer_name": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69306-750-03)", "package_ndc": "69306-750-03", "marketing_start_date": "20251107"}], "brand_name": "Diclofenac Potassium", "product_id": "69306-750_42fd182d-4a2e-7058-e063-6294a90a63f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69306-750", "generic_name": "diclofenac potassium", "labeler_name": "Doc Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA215787", "marketing_category": "ANDA", "marketing_start_date": "20241021", "listing_expiration_date": "20261231"}