Package 0054-0652-25

Brand: vigabatrin

Generic: vigabatrin
NDC Package

Package Facts

Identity

Package NDC 0054-0652-25
Digits Only 0054065225
Product NDC 0054-0652
Product ID 0054-0652_f575e137-5300-4e13-a40e-5573f6c8a066
Description

100 TABLET in 1 BOTTLE (0054-0652-25)

Marketing

Marketing Status
Marketed Since 2022-09-09
Brand vigabatrin
Generic vigabatrin
Sample Package No

Linked Drug Pages (1)

Vigabatrin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f575e137-5300-4e13-a40e-5573f6c8a066", "openfda": {"nui": ["N0000175753"], "upc": ["0300540652258"], "unii": ["GR120KRT6K"], "rxcui": ["199521"], "spl_set_id": ["5ed8d293-b7d8-4c66-9c31-8075e6f99092"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0054-0652-25)", "package_ndc": "0054-0652-25", "marketing_start_date": "20220909"}], "brand_name": "Vigabatrin", "product_id": "0054-0652_f575e137-5300-4e13-a40e-5573f6c8a066", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "0054-0652", "generic_name": "Vigabatrin", "labeler_name": "Hikma Pharmaceuticals USA Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vigabatrin", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/1"}], "application_number": "ANDA213104", "marketing_category": "ANDA", "marketing_start_date": "20220909", "listing_expiration_date": "20261231"}