Package 0904-7165-07

Brand: aminocaproic acid

Generic: aminocaproic acid
NDC Package

Package Facts

Identity

Package NDC 0904-7165-07
Digits Only 0904716507
Product NDC 0904-7165
Description

30 BLISTER PACK in 1 CARTON (0904-7165-07) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-11-30
Brand aminocaproic acid
Generic aminocaproic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "78c15c64-2046-4fa2-a82e-a27879403756", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["U6F3787206"], "rxcui": ["197351"], "spl_set_id": ["2612ee97-1723-40f2-99e6-3a736f63200f"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7165-07)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7165-07", "marketing_start_date": "20191130"}], "brand_name": "Aminocaproic acid", "product_id": "0904-7165_78c15c64-2046-4fa2-a82e-a27879403756", "dosage_form": "TABLET", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "0904-7165", "generic_name": "Aminocaproic acid", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aminocaproic acid", "active_ingredients": [{"name": "AMINOCAPROIC ACID", "strength": "500 mg/1"}], "application_number": "ANDA212492", "marketing_category": "ANDA", "marketing_start_date": "20191130", "listing_expiration_date": "20261231"}