Drugplain

Protriptyline Hydrochloride 5 mg/1

Protriptyline Hydrochloride · TABLET, FILM COATED · Epic Pharma, LLC

No Recall History
Plain English

Protriptyline Hydrochloride is a tablet, film coated containing protriptyline hydrochloride at 5 mg/1, taken oral. Manufactured by Epic Pharma, LLC.

Key Facts

Brand Name
Protriptyline Hydrochloride
Generic Name
Protriptyline Hydrochloride
NDC Code (Product)
42806-096
Manufacturer
Epic Pharma, LLC
Strength
5 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA202220
Marketing Start
01/09/2013

Recall History

No Recall History

Frequently Asked Questions

What is Protriptyline Hydrochloride used for?

Protriptyline Hydrochloride contains Protriptyline Hydrochloride. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Protriptyline Hydrochloride a controlled substance?

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

What is the generic name for Protriptyline Hydrochloride?

The generic name for Protriptyline Hydrochloride is Protriptyline Hydrochloride. There are no other listed brand versions of Protriptyline Hydrochloride.

What is the NDC code for Protriptyline Hydrochloride 5 mg/1?

The NDC (National Drug Code) for Protriptyline Hydrochloride 5 mg/1 is 42806-096, listed by Epic Pharma, LLC.

Product NDC

42806-096

Package NDC

42806-096-01

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

Data from openFDA · Public domain (CC0 1.0)