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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 203436

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NDA 203436 describes PHENTERMINE HYDROCHLORIDE, which is a drug marketed by Abc Holding, Able, Aurolife Pharma Llc, Barr, Camall, Chartwell Rx, Duramed Pharms Barr, Elite Labs, Elite Labs Inc, Invagen Pharms, Ivax Pharms, Kvk Tech, Lannett, Lannett Co Inc, Nuvo Pharm, Sandoz, Sun Pharm Industries, Teva, Tg United Inc, Upsher Smith Labs, Usl Pharma, Vitarine, Watson Labs, Zydus Pharms, Actavis Elizabeth, Aurobindo Pharma Ltd, Kvk Tech Inc, Merro Pharm Usa, Novast Labs, Prinston Inc, Sandoz Inc, Sun Pharm Inds Inc, and Actavis Labs Fl Inc, and is included in eighty-eight NDAs. It is available from thirty-one suppliers. Additional details are available on the PHENTERMINE HYDROCHLORIDE profile page.

The generic ingredient in PHENTERMINE HYDROCHLORIDE is phentermine hydrochloride; topiramate. There are seventeen drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the phentermine hydrochloride; topiramate profile page.

Summary for 203436

Tradename:	PHENTERMINE HYDROCHLORIDE
Applicant:	Kvk Tech Inc
Ingredient:	phentermine hydrochloride
Patents:	0

Pharmacology for NDA: 203436

Physiological Effect	Appetite Suppression Increased Sympathetic Activity

Suppliers and Packaging for NDA: 203436

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
PHENTERMINE HYDROCHLORIDE	phentermine hydrochloride	TABLET;ORAL	203436	ANDA	KVK-TECH, Inc.	10702-067	10702-067-03	30 TABLET in 1 BOTTLE (10702-067-03)
PHENTERMINE HYDROCHLORIDE	phentermine hydrochloride	TABLET;ORAL	203436	ANDA	KVK-TECH, Inc.	10702-067	10702-067-05	5000 TABLET in 1 BOTTLE (10702-067-05)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	8MG
Approval Date:	Mar 17, 2017	TE:	AA	RLD:	No

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