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Generated: August 17, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 086945

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NDA 086945 describes PHENTERMINE HYDROCHLORIDE, which is a drug marketed by Vitarine, Able, Usl Pharma, Sandoz Inc, Tg United Labs, Sandoz, Ken Lifescience, Abc Holding, Teva, Invagen Pharms, Aurolife Pharma Llc, Lannett, Sun Pharm Inds, Camall, Elite Labs Inc, Ivax Pharms, Upsher-smith Labs, Kvk Tech Inc, Watson Labs, Polygen Pharms, Duramed Pharms Barr, Elite Labs, Ingenus Pharms Nj, Mikah Pharma, Lannett Holdings Inc, Zydus Pharms Usa Inc, Barr, Kvk Tech, Actavis Elizabeth, Prinston Inc, Tg United Inc, and Sun Pharm Inds Inc, and is included in eighty-seven NDAs. It is available from forty-four suppliers. Additional details are available on the PHENTERMINE HYDROCHLORIDE profile page.

The generic ingredient in PHENTERMINE HYDROCHLORIDE is phentermine hydrochloride. There are seventeen drug master file entries for this compound. Forty-six suppliers are listed for this compound. Additional details are available on the phentermine hydrochloride profile page.

Summary for NDA: 086945

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Formulation / Manufacturing:see details

Pharmacology for NDA: 086945

Suppliers and Packaging for NDA: 086945

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
PHENTERMINE HYDROCHLORIDE
phentermine hydrochloride
CAPSULE;ORAL 086945 ANDA Eon Labs, Inc. 0185-5000 0185-5000-01 100 CAPSULE in 1 BOTTLE (0185-5000-01)
PHENTERMINE HYDROCHLORIDE
phentermine hydrochloride
CAPSULE;ORAL 086945 ANDA Eon Labs, Inc. 0185-5000 0185-5000-10 1000 CAPSULE in 1 BOTTLE (0185-5000-10)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength30MG
Approval Date:Jul 20, 1983TE:AARLD:No


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Serving 500+ biopharmaceutical companies globally:

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Dow

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