levetiracetam

Generic: levetiracetam

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

Drug Facts

Product Profile

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

levetiracetam 1000 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-539
Product ID 31722-539_1735a6ea-d61a-8448-e063-6394a90a5940
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090515
Listing Expiration 2026-12-31
Marketing Start 2010-10-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722539
Hyphenated Format 31722-539

Supplemental Identifiers

RxCUI
311288 311289 311290 387003
UPC
0331722539302 0331722538305 0331722537308 0331722536127 0331722539609 0331722537124 0331722536301
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 ANDA090515 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (31722-539-05)
  • 120 TABLET, FILM COATED in 1 BOTTLE (31722-539-12)
  • 30 TABLET, FILM COATED in 1 BOTTLE (31722-539-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (31722-539-60)
source: ndc

Packages (4)

31722-539-05 500 TABLET, FILM COATED in 1 BOTTLE (31722-539-05) 31722-539-12 120 TABLET, FILM COATED in 1 BOTTLE (31722-539-12) 31722-539-30 30 TABLET, FILM COATED in 1 BOTTLE (31722-539-30) 31722-539-60 60 TABLET, FILM COATED in 1 BOTTLE (31722-539-60)

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": "1735a6ea-d61a-8448-e063-6394a90a5940", "openfda": {"nui": ["N0000008486"], "upc": ["0331722539302", "0331722538305", "0331722537308", "0331722536127", "0331722539609", "0331722537124", "0331722536301"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003"], "spl_set_id": ["63b36274-89f0-42d8-9f09-f9e78e179af4"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-539-05)", "package_ndc": "31722-539-05", "marketing_start_date": "20101008"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (31722-539-12)", "package_ndc": "31722-539-12", "marketing_start_date": "20101008"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-539-30)", "package_ndc": "31722-539-30", "marketing_start_date": "20101008"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-539-60)", "package_ndc": "31722-539-60", "marketing_start_date": "20101008"}], "brand_name": "Levetiracetam", "product_id": "31722-539_1735a6ea-d61a-8448-e063-6394a90a5940", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "31722-539", "generic_name": "Levetiracetam", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "1000 mg/1"}], "application_number": "ANDA090515", "marketing_category": "ANDA", "marketing_start_date": "20101008", "listing_expiration_date": "20261231"}