Package 75907-309-30
Brand: tranexamic acid
Generic: tranexamic acidPackage Facts
Identity
Package NDC
75907-309-30
Digits Only
7590730930
Product NDC
75907-309
Description
30 TABLET in 1 BOTTLE (75907-309-30)
Marketing
Marketing Status
Brand
tranexamic acid
Generic
tranexamic acid
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e5a52dad-e328-48f2-9182-4df46f5572ef", "openfda": {"nui": ["N0000175634", "N0000175632"], "upc": ["0375907309304"], "unii": ["6T84R30KC1"], "rxcui": ["883826"], "spl_set_id": ["e5a52dad-e328-48f2-9182-4df46f5572ef"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (75907-309-30)", "package_ndc": "75907-309-30", "marketing_start_date": "20250801"}], "brand_name": "TRANEXAMIC ACID", "product_id": "75907-309_e5a52dad-e328-48f2-9182-4df46f5572ef", "dosage_form": "TABLET", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "75907-309", "generic_name": "TRANEXAMIC ACID", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRANEXAMIC ACID", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "650 mg/1"}], "application_number": "ANDA218729", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}