MIDODRINE HYDROCHLORIDE

Product NDC

68084-886

11-digit product format

680840886

Labeler code

68084

Product ID

68084-886_63226978-31f3-62a9-e053-2991aa0af510

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MIDODRINE HYDROCHLORIDE

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA076449

Marketing category

ANDA

Marketing start

2015-08-18

Marketing end

2019-03-31

Substance

MIDODRINE HYDRO

Active strength

10 mg/1

Pharmacologic classes

Adrenergic alph

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record