ALPRAZOLAM

Product NDC

61919-456

11-digit product format

619190456

Labeler code

61919

Product ID

61919-456_877120b6-029e-ba69-e053-2995a90acb1d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ALPRAZOLAM

Dosage form

TABLET

Route

ORAL

Labeler

Direct Rx

Application

ANDA200739

Marketing category

ANDA

Marketing start

2018-03-14

Marketing end

0000-00-00

Substance

ALPRAZOLAM

Active strength

1 mg/1

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record