Lorazepam

Product NDC
71205-756
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lorazepam
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA072926
Marketing category
ANDA
Substance
LORAZEPAM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71205-756-1010 TABLET in 1 BOTTLE, PLASTIC (71205-756-10) 2023-02-23NoHistorical
71205-756-1515 TABLET in 1 BOTTLE, PLASTIC (71205-756-15) 2023-02-02NoHistorical
71205-756-3030 TABLET in 1 BOTTLE, PLASTIC (71205-756-30) 2023-02-02NoHistorical
71205-756-6060 TABLET in 1 BOTTLE, PLASTIC (71205-756-60) 2023-02-02NoHistorical
71205-756-9090 TABLET in 1 BOTTLE, PLASTIC (71205-756-90) 2023-02-02NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Lorazepam Tablets, USP C-IVProficient Rx LP2023-03-01HUMAN PRESCRIPTION DRUG LABEL2