Drugplain

Humatin 250 mg/1

PAROMOMYCIN SULFATE · CAPSULE · Waylis Therapeutics LLC

No Recall History
Plain English

Humatin is a capsule containing paromomycin sulfate at 250 mg/1, taken oral. Manufactured by Waylis Therapeutics LLC.

Key Facts

Brand Name
Humatin
Generic Name
PAROMOMYCIN SULFATE
NDC Code (Product)
80725-250
Manufacturer
Waylis Therapeutics LLC
Strength
250 mg/1
Dosage Form
CAPSULE
Route
ORAL
Marketing Status
Application #
ANDA065173
Marketing Start
04/08/2021

Recall History

No Recall History

Frequently Asked Questions

What is Humatin used for?

Humatin contains PAROMOMYCIN SULFATE. It is a capsule taken oral. Consult your doctor for specific uses.

Is Humatin a controlled substance?

Humatin is not classified as a controlled substance by the DEA.

What is the generic name for Humatin?

The generic name for Humatin is PAROMOMYCIN SULFATE. There are no other listed brand versions of PAROMOMYCIN SULFATE.

What is the NDC code for Humatin 250 mg/1?

The NDC (National Drug Code) for Humatin 250 mg/1 is 80725-250, listed by Waylis Therapeutics LLC.

Product NDC

80725-250

Package NDC

80725-250-01

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

Data from openFDA · Public domain (CC0 1.0)