Package 71337-046-01

Brand: diclofenac potassium

Generic: diclofenac potassium, film coated
NDC Package

Package Facts

Identity

Package NDC 71337-046-01
Digits Only 7133704601
Product NDC 71337-046
Description

100 TABLET in 1 BOTTLE (71337-046-01)

Marketing

Marketing Status
Marketed Since 2023-06-26
Brand diclofenac potassium
Generic diclofenac potassium, film coated
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a1e049f-58f9-40e8-b7a6-bcd19ef51f75", "openfda": {"upc": ["0371337046017"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["30ab7b30-cc90-4b84-8caf-21058f1d37fa"], "manufacturer_name": ["Havix Group Inc d-b-a Aavis Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71337-046-01)", "package_ndc": "71337-046-01", "marketing_start_date": "20230626"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71337-046-05)", "package_ndc": "71337-046-05", "marketing_start_date": "20230626"}], "brand_name": "DICLOFENAC POTASSIUM", "product_id": "71337-046_2a1e049f-58f9-40e8-b7a6-bcd19ef51f75", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71337-046", "generic_name": "diclofenac potassium, film coated", "labeler_name": "Havix Group Inc d-b-a Aavis Pharmaceuticals", "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": "20230625", "listing_expiration_date": "20261231"}