Package 72336-432-12
Brand: diclofenac potassium
Generic: diclofenac potassiumPackage Facts
Identity
Package NDC
72336-432-12
Digits Only
7233643212
Product NDC
72336-432
Description
120 CAPSULE, LIQUID FILLED in 1 BOTTLE (72336-432-12)
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": "557418b9-7ce2-4f89-bc1a-f4c76ca98025", "openfda": {"upc": ["0372336432122"], "unii": ["L4D5UA6CB4"], "rxcui": ["858342"], "spl_set_id": ["90a0539a-7227-4b91-8b22-25b6f23ef35f"], "manufacturer_name": ["Lifsa Drugs LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE, LIQUID FILLED in 1 BOTTLE (72336-432-12)", "package_ndc": "72336-432-12", "marketing_start_date": "20250501"}], "brand_name": "Diclofenac Potassium", "product_id": "72336-432_557418b9-7ce2-4f89-bc1a-f4c76ca98025", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72336-432", "generic_name": "Diclofenac potassium", "labeler_name": "Lifsa Drugs LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA210078", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}