Package 0093-5031-56

Brand: tiagabine hydrochloride

Generic: tiagabine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-5031-56
Digits Only 0093503156
Product NDC 0093-5031
Product ID 0093-5031_6e4d6688-2ad2-4a19-a244-c08330649039
Description

30 TABLET, FILM COATED in 1 BOTTLE (0093-5031-56)

Marketing

Marketing Status
Marketed Since 2016-07-18
Brand tiagabine hydrochloride
Generic tiagabine hydrochloride
Sample Package No

Linked Drug Pages (1)

Tiagabine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6e4d6688-2ad2-4a19-a244-c08330649039", "openfda": {"unii": ["DQH6T6D8OY"], "rxcui": ["1299903", "1299909", "1299911", "1299917"], "spl_set_id": ["953ef3cc-e3cb-480f-b9ea-256520fd62b8"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-5031-56)", "package_ndc": "0093-5031-56", "marketing_start_date": "20160718"}], "brand_name": "Tiagabine Hydrochloride", "product_id": "0093-5031_6e4d6688-2ad2-4a19-a244-c08330649039", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0093-5031", "generic_name": "Tiagabine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tiagabine Hydrochloride", "active_ingredients": [{"name": "TIAGABINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "NDA020646", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160603", "listing_expiration_date": "20261231"}