Alprazolam

Product NDC
55154-4979
11-digit product format
551544979
Labeler code
55154
Product ID
55154-4979_845c75dd-5b7e-4c1e-8830-8b814cbed9e4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Alprazolam
Dosage form
TABLET
Route
ORAL
Labeler
Cardinal Health
Application
ANDA074112
Marketing category
ANDA
Marketing start
2013-09-04
Marketing end
0000-00-00
Substance
ALPRAZOLAM
Active strength
0 mg/1
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
YU55MQ3IZYALPRAZOLAM28981-97-7ALPRAZOLAM