Alprazolam

Product NDC
76420-666
11-digit product format
764200666
Labeler code
76420
Product ID
76420-666_0ea9692e-7d75-80f3-e063-6294a90ad6f9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
alprazolam
Dosage form
TABLET
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
NDA018276
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
1981-10-16
Substance
ALPRAZOLAM
Active strength
2 mg/1
Pharmacologic classes
Benzodiazepine [EPC], Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
YU55MQ3IZYALPRAZOLAM28981-97-7ALPRAZOLAM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76420-666-0176420066601100 TABLET in 1 BOTTLE (76420-666-01) 100 tablet2024-01-11NoNoHistorical
76420-666-307642006663030 TABLET in 1 BOTTLE (76420-666-30) 30 tablet2024-01-11NoNoHistorical
76420-666-607642006666060 TABLET in 1 BOTTLE (76420-666-60) 60 tablet2024-01-11NoNoHistorical
76420-666-907642006669090 TABLET in 1 BOTTLE (76420-666-90) 90 tablet2024-01-11NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AlprazolamAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2024-01-11HUMAN PRESCRIPTION DRUG LABEL1