United States · FDA National Drug Code directory

LORAZEPAM

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
13107-084_67012944-0947-4e64-adab-869993f2f709
Product NDC
13107-084
Form
TABLET
Composition / generic term
LORAZEPAM
Labeler
Aurolife Pharma LLC
Marketing category
ANDA
Marketing start / end (source format)
20210201
Source listing expiry
20261231

Source-listed ingredients

  • LORAZEPAM — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (13107-084-01) · 13107-084-01
  • 500 TABLET in 1 BOTTLE (13107-084-05) · 13107-084-05
  • 10 TABLET in 1 BOTTLE (13107-084-10) · 13107-084-10
  • 1000 TABLET in 1 BOTTLE (13107-084-99) · 13107-084-99

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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