Package 10135-806-01
Brand: diclofenac potassium
Generic: diclofenac potassiumPackage Facts
Identity
Package NDC
10135-806-01
Digits Only
1013580601
Product NDC
10135-806
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-806-01)
Marketing
Marketing Status
Brand
diclofenac potassium
Generic
diclofenac potassium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30c7197b-7111-d8a7-e063-6394a90addfb", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["30c7197b-7110-d8a7-e063-6394a90addfb"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-806-01)", "package_ndc": "10135-806-01", "marketing_start_date": "20250301"}], "brand_name": "Diclofenac Potassium", "product_id": "10135-806_30c7197b-7111-d8a7-e063-6394a90addfb", "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": "10135-806", "generic_name": "diclofenac potassium", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA075463", "marketing_category": "ANDA", "marketing_start_date": "20250301", "listing_expiration_date": "20261231"}