Terazosin

Product NDC

68788-9673

11-digit product format

687889673

Labeler code

68788

Product ID

68788-9673_3ee028dd-e6c0-490b-baa8-8eeba48ab88c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Terazosin

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals

Application

ANDA075498

Marketing category

ANDA

Marketing start

2013-07-12

Marketing end

0000-00-00

Substance

TERAZOSIN HYDRO

Active strength

5 mg/1

Pharmacologic classes

Adrenergic alph

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record