Drugplain

Ibandronate Sodium 150 mg/1

Ibandronate Sodium · TABLET, FILM COATED · Aurobindo Pharma Limited

No Recall History
Plain English

Ibandronate sodium is an oral medication taken as a tablet to treat and prevent osteoporosis, a condition where bones become weak and brittle. It works by slowing bone loss to help maintain bone strength and reduce the risk of fractures.

Key Facts

Brand Name
Ibandronate Sodium
Generic Name
Ibandronate Sodium
NDC Code (Product)
65862-237
Manufacturer
Aurobindo Pharma Limited
Strength
150 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA204502
Marketing Start
03/11/2016

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

arthralgia250 reports
diarrhoea238 reports
nausea227 reports
femur fracture218 reports
headache205 reports
fatigue200 reports
fall170 reports
dizziness169 reports
pain164 reports
asthenia155 reports

Frequently Asked Questions

What is Ibandronate Sodium used for?

Ibandronate sodium is an oral medication taken as a tablet to treat and prevent osteoporosis, a condition where bones become weak and brittle. It works by slowing bone loss to help maintain bone strength and reduce the risk of fractures.

Is Ibandronate Sodium a controlled substance?

Ibandronate Sodium is not classified as a controlled substance by the DEA.

What is the generic name for Ibandronate Sodium?

The generic name for Ibandronate Sodium is Ibandronate Sodium. There are 8 other brand versions of Ibandronate Sodium.

What is the NDC code for Ibandronate Sodium 150 mg/1?

The NDC (National Drug Code) for Ibandronate Sodium 150 mg/1 is 65862-237, listed by Aurobindo Pharma Limited.