levetiracetam

Generic: levetiracetam

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

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler armas pharmaceuticals inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

levetiracetam 100 mg/mL

Manufacturer
Armas Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 72485-106
Product ID 72485-106_19255a4c-a8da-4e24-9633-16b9e3fc1f89
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211954
Listing Expiration 2026-12-31
Marketing Start 2021-01-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72485106
Hyphenated Format 72485-106

Supplemental Identifiers

RxCUI
647121
UPC
0372485106011
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 ANDA211954 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (72485-106-10) / 5 mL in 1 VIAL, SINGLE-DOSE (72485-106-01)
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (72485-106-25) / 5 mL in 1 VIAL, SINGLE-DOSE (72485-106-01)
source: ndc

Packages (2)

Ingredients (1)

levetiracetam (100 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "19255a4c-a8da-4e24-9633-16b9e3fc1f89", "openfda": {"nui": ["N0000008486"], "upc": ["0372485106011"], "unii": ["44YRR34555"], "rxcui": ["647121"], "spl_set_id": ["7be45c40-8d75-4c40-97a4-95067129bc2a"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Armas Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (72485-106-10)  / 5 mL in 1 VIAL, SINGLE-DOSE (72485-106-01)", "package_ndc": "72485-106-10", "marketing_start_date": "20210114"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (72485-106-25)  / 5 mL in 1 VIAL, SINGLE-DOSE (72485-106-01)", "package_ndc": "72485-106-25", "marketing_start_date": "20230316"}], "brand_name": "LEVETIRACETAM", "product_id": "72485-106_19255a4c-a8da-4e24-9633-16b9e3fc1f89", "dosage_form": "INJECTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72485-106", "generic_name": "LEVETIRACETAM", "labeler_name": "Armas Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVETIRACETAM", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "100 mg/mL"}], "application_number": "ANDA211954", "marketing_category": "ANDA", "marketing_start_date": "20210114", "listing_expiration_date": "20261231"}