Lorazepam

Product NDC
60687-401
11-digit product format
606870401
Labeler code
60687
Product ID
60687-401_de596660-e512-2754-e053-2995a90adc63
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lorazepam
Dosage form
TABLET
Route
ORAL
Labeler
American Health Packaging
Application
ANDA072926
Marketing category
ANDA
Marketing start
2020-06-17
Marketing end
2022-11-30
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
60687-401-01EA - Each60687-40188f04823-8073-412f-81e3-031ad0defbd412020-07-13
60687-401-11EA - Each60687-401a3c625eb-29ef-4c19-bab0-6ecd0c44c36c12020-07-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60687-401-0160687040101100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-401-01) > 1 TABLET in 1 BLISTER PACK (60687-401-11) 100 blister pack2020-06-170000-00-00NoNoCurrent