levetiracetam

Generic: levetiracetam

Labeler: exelan pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler exelan pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levetiracetam 750 mg/1

Manufacturer
Exelan Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 76282-248
Product ID 76282-248_b044e723-e969-45fa-a4e6-159bfb65267a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078234
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 76282248
Hyphenated Format 76282-248

Supplemental Identifiers

RxCUI
311288 311289 311290
UPC
0376282248127 0376282247120 0376282246123
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 ANDA078234 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 120 TABLET in 1 BOTTLE (76282-248-12)
source: ndc

Packages (1)

76282-248-12 120 TABLET in 1 BOTTLE (76282-248-12)

Ingredients (1)

levetiracetam (750 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": "b044e723-e969-45fa-a4e6-159bfb65267a", "openfda": {"nui": ["N0000008486"], "upc": ["0376282248127", "0376282247120", "0376282246123"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290"], "spl_set_id": ["28c0e61e-1af9-410a-9fa9-b71bf99a776b"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Exelan Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (76282-248-12)", "package_ndc": "76282-248-12", "marketing_start_date": "20090115"}], "brand_name": "Levetiracetam", "product_id": "76282-248_b044e723-e969-45fa-a4e6-159bfb65267a", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "76282-248", "generic_name": "Levetiracetam", "labeler_name": "Exelan Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "750 mg/1"}], "application_number": "ANDA078234", "marketing_category": "ANDA", "marketing_start_date": "20090115", "listing_expiration_date": "20261231"}