ALPRAZOLAM

Product NDC

61919-862

11-digit product format

619190862

Labeler code

61919

Product ID

61919-862_87d379da-103c-c751-e053-2995a90a56de

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ALPRAZOLAM

Dosage form

TABLET

Route

ORAL

Labeler

DIRECT RX

Application

ANDA074909

Marketing category

ANDA

Marketing start

2019-05-01

Marketing end

0000-00-00

Substance

ALPRAZOLAM

Active strength

2 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