Drugplain

Naftifine Hydrochloride 20 mg/g

Naftifine Hydrochloride · GEL · Sun Pharmaceutical Industries, Inc.

No Recall History
Plain English

Naftifine Hydrochloride is a gel containing naftifine hydrochloride at 20 mg/g, taken topical. Manufactured by Sun Pharmaceutical Industries, Inc..

Key Facts

Brand Name
Naftifine Hydrochloride
Generic Name
Naftifine Hydrochloride
NDC Code (Product)
51672-1376
Manufacturer
Sun Pharmaceutical Industries, Inc.
Strength
20 mg/g
Dosage Form
GEL
Route
TOPICAL
Marketing Status
Application #
ANDA208201
Marketing Start
04/01/2023

Recall History

No Recall History

Frequently Asked Questions

What is Naftifine Hydrochloride used for?

Naftifine Hydrochloride contains Naftifine Hydrochloride. It is a gel taken topical. Consult your doctor for specific uses.

Is Naftifine Hydrochloride a controlled substance?

Naftifine Hydrochloride is not classified as a controlled substance by the DEA.

What is the generic name for Naftifine Hydrochloride?

The generic name for Naftifine Hydrochloride is Naftifine Hydrochloride. There are 2 other brand versions of Naftifine Hydrochloride.

What is the NDC code for Naftifine Hydrochloride 20 mg/g?

The NDC (National Drug Code) for Naftifine Hydrochloride 20 mg/g is 51672-1376, listed by Sun Pharmaceutical Industries, Inc..

Product NDC

51672-1376

Package NDC

51672-1376-3

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

Data from openFDA · Public domain (CC0 1.0)