Package 49884-358-03

Brand: vigabatrin

Generic: vigabatrin
NDC Package

Package Facts

Identity

Package NDC 49884-358-03
Digits Only 4988435803
Product NDC 49884-358
Product ID 49884-358_85f80498-dbd9-46e7-bac8-72db25a0ef22
Description

50 PACKET in 1 CARTON (49884-358-03) / 10 mL in 1 PACKET (49884-358-52)

Marketing

Marketing Status
Marketed Since 2017-04-27
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": "85f80498-dbd9-46e7-bac8-72db25a0ef22", "openfda": {"nui": ["N0000175753"], "upc": ["0349884358037", "0349884358525"], "unii": ["GR120KRT6K"], "rxcui": ["250820"], "spl_set_id": ["e7cbc0a5-8c28-4451-9176-b608e228ba66"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["ENDO USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 CARTON (49884-358-03)  / 10 mL in 1 PACKET (49884-358-52)", "package_ndc": "49884-358-03", "marketing_start_date": "20170427"}], "brand_name": "VIGABATRIN", "product_id": "49884-358_85f80498-dbd9-46e7-bac8-72db25a0ef22", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "49884-358", "generic_name": "vigabatrin", "labeler_name": "ENDO USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VIGABATRIN", "active_ingredients": [{"name": "VIGABATRIN", "strength": "50 mg/mL"}], "application_number": "ANDA208218", "marketing_category": "ANDA", "marketing_start_date": "20170427", "listing_expiration_date": "20261231"}