Package 43598-651-01

Brand: vigabatrin

Generic: vigabatrin
NDC Package

Package Facts

Identity

Package NDC 43598-651-01
Digits Only 4359865101
Product NDC 43598-651
Product ID 43598-651_f9d29bec-f73b-7dc9-5f1b-7857dc0fdb74
Description

100 TABLET, FILM COATED in 1 BOTTLE (43598-651-01)

Marketing

Marketing Status
Marketed Since 2021-02-01
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": "f9d29bec-f73b-7dc9-5f1b-7857dc0fdb74", "openfda": {"nui": ["N0000175753"], "upc": ["0343598651019"], "unii": ["GR120KRT6K"], "rxcui": ["199521"], "spl_set_id": ["0afdc84c-f8ec-330a-31c9-fac4ed256931"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Dr. Reddys Laboratories Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (43598-651-01)", "package_ndc": "43598-651-01", "marketing_start_date": "20210201"}], "brand_name": "Vigabatrin", "product_id": "43598-651_f9d29bec-f73b-7dc9-5f1b-7857dc0fdb74", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]"], "product_ndc": "43598-651", "generic_name": "Vigabatrin", "labeler_name": "Dr. Reddys Laboratories Inc.,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vigabatrin", "active_ingredients": [{"name": "VIGABATRIN", "strength": "500 mg/1"}], "application_number": "ANDA211539", "marketing_category": "ANDA", "marketing_start_date": "20210201", "listing_expiration_date": "20261231"}