Package 81033-013-50

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 81033-013-50
Digits Only 8103301350
Product NDC 81033-013
Description

50 CUP, UNIT-DOSE in 1 CARTON (81033-013-50) / 5 mL in 1 CUP, UNIT-DOSE (81033-013-05)

Marketing

Marketing Status
Marketed Since 2025-03-01
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": "30a4626d-74f4-6385-e063-6394a90a2950", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["403884"], "spl_set_id": ["30a4626d-74f3-6385-e063-6394a90a2950"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CARTON (81033-013-50)  / 5 mL in 1 CUP, UNIT-DOSE (81033-013-05)", "package_ndc": "81033-013-50", "marketing_start_date": "20250301"}], "brand_name": "LEVETIRACETAM", "product_id": "81033-013_30a4626d-74f4-6385-e063-6394a90a2950", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "81033-013", "generic_name": "LEVETIRACETAM", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVETIRACETAM", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "100 mg/mL"}], "application_number": "ANDA079120", "marketing_category": "ANDA", "marketing_start_date": "20240718", "listing_expiration_date": "20261231"}