Acarbose

Product NDC

55289-171

11-digit product format

552890171

Labeler code

55289

Product ID

55289-171_7b97fb7a-e7ef-0e07-e053-2991aa0a813c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acarbose

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA078470

Marketing category

ANDA

Marketing start

2008-05-07

Marketing end

0000-00-00

Substance

ACARBOSE

Active strength

50 mg/1

Pharmacologic classes

alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record