levetiracetam
Generic: levetiracetam
Labeler: dr. reddy's laboratories limitedDrug Facts
Product Profile
Brand Name
levetiracetam
Generic Name
levetiracetam
Labeler
dr. reddy's laboratories limited
Dosage Form
TABLET
Routes
Active Ingredients
levetiracetam 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55111-183
Product ID
55111-183_2de4ebba-b125-4355-35f5-69b92e56634b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076920
Listing Expiration
2026-12-31
Marketing Start
2009-01-15
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55111183
Hyphenated Format
55111-183
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
levetiracetam (source: ndc)
Generic Name
levetiracetam (source: ndc)
Application Number
ANDA076920 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (55111-183-01)
- 120 TABLET in 1 BOTTLE (55111-183-04)
- 500 TABLET in 1 BOTTLE (55111-183-05)
- 30 TABLET in 1 BOTTLE (55111-183-30)
- 1 BLISTER PACK in 1 CARTON (55111-183-79) / 10 TABLET in 1 BLISTER PACK
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2de4ebba-b125-4355-35f5-69b92e56634b", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290"], "spl_set_id": ["ee03507b-cb35-4fe9-ae7b-85ea89f876f0"], "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 (55111-183-01)", "package_ndc": "55111-183-01", "marketing_start_date": "20090115"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (55111-183-04)", "package_ndc": "55111-183-04", "marketing_start_date": "20090115"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-183-05)", "package_ndc": "55111-183-05", "marketing_start_date": "20090115"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-183-30)", "package_ndc": "55111-183-30", "marketing_start_date": "20090115"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (55111-183-79) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "55111-183-79", "marketing_start_date": "20090115"}], "brand_name": "Levetiracetam", "product_id": "55111-183_2de4ebba-b125-4355-35f5-69b92e56634b", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "55111-183", "generic_name": "Levetiracetam", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "750 mg/1"}], "application_number": "ANDA076920", "marketing_category": "ANDA", "marketing_start_date": "20090115", "listing_expiration_date": "20261231"}