Package 70512-900-30

Brand: diclofenac potassium

Generic: diclofenac potassium
NDC Package

Package Facts

Identity

Package NDC 70512-900-30
Digits Only 7051290030
Product NDC 70512-900
Product ID 70512-900_457251ae-4588-3ba1-e063-6394a90ab981
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70512-900-30)

Marketing

Marketing Status
Marketed Since 2024-11-01
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": "457251ae-4588-3ba1-e063-6394a90ab981", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["26bf3a4a-42c6-cb59-e063-6394a90abd8b"], "manufacturer_name": ["SOLA Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70512-900-30)", "package_ndc": "70512-900-30", "marketing_start_date": "20241101"}], "brand_name": "Diclofenac Potassium", "product_id": "70512-900_457251ae-4588-3ba1-e063-6394a90ab981", "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": "70512-900", "generic_name": "diclofenac potassium", "labeler_name": "SOLA Pharmaceuticals, LLC", "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": "20241101", "listing_expiration_date": "20261231"}