Package 29300-116-10
Brand: topiramate
Generic: topiramatePackage Facts
Identity
Package NDC
29300-116-10
Digits Only
2930011610
Product NDC
29300-116
Description
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-116-10)
Marketing
Marketing Status
Brand
topiramate
Generic
topiramate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b609e53c-2d69-4437-b2a1-9f322208eb27", "openfda": {"nui": ["N0000008486", "N0000185506", "N0000182140"], "upc": ["0329300118162"], "unii": ["0H73WJJ391"], "rxcui": ["151226", "199888", "199889", "199890"], "spl_set_id": ["6ee00e82-799d-445e-b658-a9712c49a28e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_moa": ["Cytochrome P450 3A4 Inducers [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-116-01)", "package_ndc": "29300-116-01", "marketing_start_date": "20130701"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-116-05)", "package_ndc": "29300-116-05", "marketing_start_date": "20130701"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-116-10)", "package_ndc": "29300-116-10", "marketing_start_date": "20130701"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-116-16)", "package_ndc": "29300-116-16", "marketing_start_date": "20130701"}], "brand_name": "topiramate", "product_id": "29300-116_b609e53c-2d69-4437-b2a1-9f322208eb27", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Cytochrome P450 3A4 Inducers [MoA]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "29300-116", "generic_name": "topiramate", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "topiramate", "active_ingredients": [{"name": "TOPIRAMATE", "strength": "50 mg/1"}], "application_number": "ANDA090162", "marketing_category": "ANDA", "marketing_start_date": "20130701", "listing_expiration_date": "20261231"}