Package 55111-248-30

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 55111-248-30
Digits Only 5511124830
Product NDC 55111-248
Description

30 TABLET in 1 BOTTLE (55111-248-30)

Marketing

Marketing Status
Marketed Since 2009-01-15
Brand levetiracetam
Generic levetiracetam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b3acece-e7d3-2b1f-db18-77e04f6d7918", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["387003"], "spl_set_id": ["1f3c04d9-cccb-06a3-a0f3-f7c9228ee743"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-248-01)", "package_ndc": "55111-248-01", "marketing_start_date": "20090115"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-248-05)", "package_ndc": "55111-248-05", "marketing_start_date": "20090115"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-248-30)", "package_ndc": "55111-248-30", "marketing_start_date": "20090115"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (55111-248-60)", "package_ndc": "55111-248-60", "marketing_start_date": "20090115"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (55111-248-79)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "55111-248-79", "marketing_start_date": "20090115"}], "brand_name": "Levetiracetam", "product_id": "55111-248_1b3acece-e7d3-2b1f-db18-77e04f6d7918", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "55111-248", "generic_name": "Levetiracetam", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "1000 mg/1"}], "application_number": "ANDA078904", "marketing_category": "ANDA", "marketing_start_date": "20090115", "listing_expiration_date": "20261231"}