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
- 68788-7355_b4dfa37c-fc4b-4ee1-b674-9ed0d9b118ad
- Product NDC
- 68788-7355
- Form
- TABLET
- Composition / generic term
- Lorazepam
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190227
- Source listing expiry
- 20271231
Source-listed ingredients
- LORAZEPAM — .5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (68788-7355-1) · 68788-7355-1
- 30 TABLET in 1 BOTTLE (68788-7355-3) · 68788-7355-3
- 60 TABLET in 1 BOTTLE (68788-7355-6) · 68788-7355-6
- 120 TABLET in 1 BOTTLE (68788-7355-8) · 68788-7355-8
- 90 TABLET in 1 BOTTLE (68788-7355-9) · 68788-7355-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →