Package 70771-1742-8

Brand: vigabatrin

Generic: vigabatrin
NDC Package

Package Facts

Identity

Package NDC 70771-1742-8
Digits Only 7077117428
Product NDC 70771-1742
Product ID 70771-1742_2fd46d14-d59a-4335-9f92-9e029defc7b2
Description

50 PACKET in 1 CARTON (70771-1742-8) / 10 mL in 1 PACKET (70771-1742-1)

Marketing

Marketing Status
Marketed Since 2025-03-24
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": "2fd46d14-d59a-4335-9f92-9e029defc7b2", "openfda": {"nui": ["N0000175753"], "unii": ["GR120KRT6K"], "rxcui": ["250820"], "spl_set_id": ["cd5ebc7a-8d5b-46b4-ad9b-e4a25fa3e26c"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 CARTON (70771-1742-8)  / 10 mL in 1 PACKET (70771-1742-1)", "package_ndc": "70771-1742-8", "marketing_start_date": "20250324"}], "brand_name": "vigabatrin", "product_id": "70771-1742_2fd46d14-d59a-4335-9f92-9e029defc7b2", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "70771-1742", "generic_name": "vigabatrin", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vigabatrin", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/10mL"}], "application_number": "ANDA214671", "marketing_category": "ANDA", "marketing_start_date": "20250324", "listing_expiration_date": "20261231"}