Precose

Product NDC

50419-862

11-digit product format

504190862

Labeler code

50419

Product ID

50419-862_61dbcee7-11a4-4d8c-8e2c-7cbab79b2871

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acarbose

Dosage form

TABLET

Route

ORAL

Labeler

Bayer HealthCare Pharmaceuticals Inc.

Application

NDA020482

Marketing category

NDA

Marketing start

2008-01-30

Marketing end

0000-00-00

Substance

ACARBOSE

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record