Alprazolam

Product NDC

69452-112

11-digit product format

694520112

Labeler code

69452

Product ID

69452-112_c8370c52-608f-492a-96b1-cc22a5f44035

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alprazolam

Dosage form

TABLET

Route

ORAL

Labeler

Bionpharma Inc.

Application

ANDA200739

Marketing category

ANDA

Marketing start

2015-10-01

Marketing end

2019-03-31

Substance

ALPRAZOLAM

Active strength

1 mg/1

Pharmacologic classes

Benzodiazepine

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record