Alendronate Sodium

Product NDC

68788-7393

11-digit product format

687887393

Labeler code

68788

Product ID

68788-7393_e973e057-33f4-406c-bd7d-9e954064b4a6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alendronate Sodium

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA075710

Marketing category

ANDA

Marketing start

2016-09-28

Marketing end

0000-00-00

Substance

ALENDRONATE SODIUM

Active strength

70 mg/1

Pharmacologic classes

Bisphosphonate [EPC],Diphosphonates [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record