Ibandronate sodium

Product NDC

23155-162

11-digit product format

231550162

Labeler code

23155

Product ID

23155-162_54180f55-2fb9-468a-9b68-841b9070a395

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ibandronate sodium

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Heritage Pharmaceuticals Inc.

Application

ANDA203987

Marketing category

ANDA

Marketing start

2014-09-04

Marketing end

0000-00-00

Substance

IBANDRONATE SODIUM

Active strength

3 mg/3mL

Pharmacologic classes

Bisphosphonate [EPC],Diphosphonates [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record