levetiracetam

Generic: levetiracetam

Labeler: dr. reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler dr. reddy's laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levetiracetam 1000 mg/1

Manufacturer
Dr. Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-248
Product ID 55111-248_1b3acece-e7d3-2b1f-db18-77e04f6d7918
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078904
Listing Expiration 2026-12-31
Marketing Start 2009-01-15

Pharmacologic Class

Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55111248
Hyphenated Format 55111-248

Supplemental Identifiers

RxCUI
387003
UNII
44YRR34555
NUI
N0000008486

Packaging Origin

Original Packager
true

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 ANDA078904 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (55111-248-01)
  • 500 TABLET in 1 BOTTLE (55111-248-05)
  • 30 TABLET in 1 BOTTLE (55111-248-30)
  • 60 TABLET in 1 BOTTLE (55111-248-60)
  • 1 BLISTER PACK in 1 CARTON (55111-248-79) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (5)

55111-248-01 100 TABLET in 1 BOTTLE (55111-248-01) 55111-248-05 500 TABLET in 1 BOTTLE (55111-248-05) 55111-248-30 30 TABLET in 1 BOTTLE (55111-248-30) 55111-248-60 60 TABLET in 1 BOTTLE (55111-248-60) 55111-248-79 1 BLISTER PACK in 1 CARTON (55111-248-79) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

levetiracetam (1000 mg/1)

Linked Drug Pages (1)

Levetiracetam ndc-match (0.9)

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"}