Package 70771-1654-1

Brand: vigabatrin

Generic: vigabatrin
NDC Package

Package Facts

Identity

Package NDC 70771-1654-1
Digits Only 7077116541
Product NDC 70771-1654
Product ID 70771-1654_5eea977c-802f-4fdf-9ad3-70a4e2f1cf1d
Description

100 TABLET, FILM COATED in 1 BOTTLE (70771-1654-1)

Marketing

Marketing Status
Marketed Since 2022-01-20
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": "5eea977c-802f-4fdf-9ad3-70a4e2f1cf1d", "openfda": {"nui": ["N0000175753"], "unii": ["GR120KRT6K"], "rxcui": ["199521"], "spl_set_id": ["e9c99000-fc0c-4083-b620-ba9ac821f8ac"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1654-1)", "package_ndc": "70771-1654-1", "marketing_start_date": "20220120"}], "brand_name": "vigabatrin", "product_id": "70771-1654_5eea977c-802f-4fdf-9ad3-70a4e2f1cf1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "70771-1654", "generic_name": "vigabatrin", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vigabatrin", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/1"}], "application_number": "ANDA215707", "marketing_category": "ANDA", "marketing_start_date": "20220120", "listing_expiration_date": "20261231"}