Lorazepam

Product NDC
60687-355
11-digit product format
606870355
Labeler code
60687
Product ID
60687-355_de596660-e512-2754-e053-2995a90adc63
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lorazepam
Dosage form
TABLET
Route
ORAL
Labeler
American Health Packaging
Application
ANDA072927
Marketing category
ANDA
Marketing start
2020-02-17
Marketing end
2023-03-31
Substance
LORAZEPAM
Active strength
1 mg/1
Pharmacologic classes
Benzodiazepine [EPC], Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60687-355-01EA - Each60687-3552cebf9d3-e194-47a3-859e-6451ffa7166612020-03-10
60687-355-11EA - Each60687-355767cecf8-7c7e-4542-928d-3c1ca46687b712020-03-10

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60687-355-0160687035501100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-355-01) > 1 TABLET in 1 BLISTER PACK (60687-355-11) 100 blister pack2020-02-170000-00-00NoNoCurrent