ISOXSUPRINE HYDROCHLORIDE

Product NDC

42582-100

11-digit product format

425820100

Labeler code

42582

Product ID

42582-100_44838a95-745c-4ee2-8361-e3fd9f3de1de

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

isoxsuprine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Bi-Coastal Pharmaceutical Corporation

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2011-06-02

Marketing end

0000-00-00

Substance

ISOXSUPRINE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record