Tamsulosin Hydrochloride

Product NDC

68788-0816

11-digit product format

687880816

Labeler code

68788

Product ID

68788-0816_a6cdfd0e-a3f2-4b9d-adab-8104099dab24

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tamsulosin Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals

Application

ANDA078938

Marketing category

ANDA

Marketing start

2010-10-07

Marketing end

0000-00-00

Substance

TAMSULOSIN HYDR

Active strength

0 mg/1

Pharmacologic classes

Adrenergic alph

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record