Package 70771-1078-8
Brand: felbamate
Generic: felbamatePackage Facts
Identity
Package NDC
70771-1078-8
Digits Only
7077110788
Product NDC
70771-1078
Description
180 TABLET in 1 BOTTLE (70771-1078-8)
Marketing
Marketing Status
Brand
felbamate
Generic
felbamate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "785f1747-e29d-432a-82e7-fcaeea202327", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["X72RBB02N8"], "rxcui": ["198358", "198359"], "spl_set_id": ["efa55cb2-b625-4392-9ddb-0a8ad8ee58c4"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1078-1)", "package_ndc": "70771-1078-1", "marketing_start_date": "20170815"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70771-1078-3)", "package_ndc": "70771-1078-3", "marketing_start_date": "20170815"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1078-4) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "70771-1078-4", "marketing_start_date": "20170815"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1078-5)", "package_ndc": "70771-1078-5", "marketing_start_date": "20170815"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (70771-1078-8)", "package_ndc": "70771-1078-8", "marketing_start_date": "20170815"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70771-1078-9)", "package_ndc": "70771-1078-9", "marketing_start_date": "20170815"}], "brand_name": "Felbamate", "product_id": "70771-1078_785f1747-e29d-432a-82e7-fcaeea202327", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70771-1078", "generic_name": "Felbamate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felbamate", "active_ingredients": [{"name": "FELBAMATE", "strength": "600 mg/1"}], "application_number": "ANDA208970", "marketing_category": "ANDA", "marketing_start_date": "20170815", "listing_expiration_date": "20261231"}