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
- 71205-228_08a911c9-3b1b-4404-a770-5bf4d27c7e96
- Product NDC
- 71205-228
- Form
- TABLET
- Composition / generic term
- Lorazepam
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170324
- Source listing expiry
- 20261231
Source-listed ingredients
- LORAZEPAM — .5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET in 1 BOTTLE (71205-228-02) · 71205-228-02
- 3 TABLET in 1 BOTTLE (71205-228-03) · 71205-228-03
- 15 TABLET in 1 BOTTLE (71205-228-15) · 71205-228-15
- 20 TABLET in 1 BOTTLE (71205-228-20) · 71205-228-20
- 30 TABLET in 1 BOTTLE (71205-228-30) · 71205-228-30
- 60 TABLET in 1 BOTTLE (71205-228-60) · 71205-228-60
- 90 TABLET in 1 BOTTLE (71205-228-90) · 71205-228-90
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 →