Drugplain

Galantamine Hydrobromide 16 mg/1

Galantamine Hydrobromide · CAPSULE, EXTENDED RELEASE · Sun Pharmaceutical Industries, Inc.

No Recall History
Plain English

Galantamine Hydrobromide is a capsule, extended release containing galantamine hydrobromide at 16 mg/1, taken oral. Manufactured by Sun Pharmaceutical Industries, Inc..

Key Facts

Brand Name
Galantamine Hydrobromide
Generic Name
Galantamine Hydrobromide
NDC Code (Product)
47335-836
Manufacturer
Sun Pharmaceutical Industries, Inc.
Strength
16 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA090178
Marketing Start
02/09/2011

Recall History

No Recall History

Side Effects Reported to FDA

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

fall494 reports
constipation417 reports
cognitive disorder414 reports
hypotension405 reports
orthostatic hypotension403 reports
balance disorder402 reports
sedation380 reports
depressed level of consciousness374 reports
pain364 reports
creatinine renal clearance decreased359 reports

Frequently Asked Questions

What is Galantamine Hydrobromide used for?

Galantamine Hydrobromide contains Galantamine Hydrobromide. It is a capsule, extended release taken oral. Consult your doctor for specific uses.

Is Galantamine Hydrobromide a controlled substance?

Galantamine Hydrobromide is not classified as a controlled substance by the DEA.

What is the generic name for Galantamine Hydrobromide?

The generic name for Galantamine Hydrobromide is Galantamine Hydrobromide. There are no other listed brand versions of Galantamine Hydrobromide.

What is the NDC code for Galantamine Hydrobromide 16 mg/1?

The NDC (National Drug Code) for Galantamine Hydrobromide 16 mg/1 is 47335-836, listed by Sun Pharmaceutical Industries, Inc..

Product NDC

47335-836

Package NDC

47335-836-08

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)