NDC 71610-122 – Lorazepam

Lorazepam 1 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71610-122

Product details

Brand name
Lorazepam
Generic name
Lorazepam
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078203
Marketed since
October 9, 2009
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Lorazepam →

Package NDC codes (12)

Package NDCDescriptionSince
71610-122-1010 TABLET in 1 BOTTLE (71610-122-10)Aug 15, 2018
71610-122-1515 TABLET in 1 BOTTLE (71610-122-15)Aug 15, 2018
71610-122-2020 TABLET in 1 BOTTLE (71610-122-20)Oct 3, 2018
71610-122-2828 TABLET in 1 BOTTLE (71610-122-28)Dec 21, 2023
71610-122-3030 TABLET in 1 BOTTLE (71610-122-30)Oct 3, 2018
71610-122-4545 TABLET in 1 BOTTLE (71610-122-45)Oct 3, 2018
71610-122-5360 TABLET in 1 BOTTLE (71610-122-53)Oct 3, 2018
71610-122-5575 TABLET in 1 BOTTLE (71610-122-55)Nov 26, 2019
71610-122-6090 TABLET in 1 BOTTLE (71610-122-60)Oct 3, 2018
71610-122-70120 TABLET in 1 BOTTLE (71610-122-70)Aug 15, 2018
71610-122-75150 TABLET in 1 BOTTLE (71610-122-75)Jan 7, 2019
71610-122-80180 TABLET in 1 BOTTLE (71610-122-80)Oct 3, 2018

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