alendronate sodium

Product NDC

70518-0269

11-digit product format

705180269

Labeler code

70518

Product ID

70518-0269_835e4863-315a-ffa7-e053-2991aa0aa0b0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

alendronate sodium

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076984

Marketing category

ANDA

Marketing start

2017-05-04

Marketing end

0000-00-00

Substance

ALENDRONATE SODIUM

Active strength

70 mg/1

Pharmacologic classes

Bisphosphonate [EPC],Diphosphonates [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record