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Mallinckrodt
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Generated: October 19, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 071972

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NDA 071972 describes PROPRANOLOL HYDROCHLORIDE, which is a drug marketed by Inwood Labs, Sandoz Inc, Rp Scherer, Anda Repository, Duramed Pharms Barr, Upsher-smith Labs, Mylan, Northstar Hlthcare, Purepac Pharm, Superpharm, Roxane, Lederle, Vintage Pharms, Baxter Hlthcare Corp, Schering, Zydus Pharms Usa Inc, Dava Pharms Inc, Fresenius Kabi Usa, Teva, Smith And Nephew, Solopak, Warner Chilcott, Watson Labs, Watson Labs Teva, Ipca Labs Ltd, Sandoz, Hikma Farmaceutica, Ivax Sub Teva Pharms, Nortec Dev Assoc, Interpharm, Impax Labs Inc, Ani Pharms Inc, West-ward Pharms Int, Morton Grove, Par Pharm, Athenex Inc, and Actavis Elizabeth, and is included in one hundred and forty-nine NDAs. It is available from fifty suppliers. Additional details are available on the PROPRANOLOL HYDROCHLORIDE profile page.

The generic ingredient in PROPRANOLOL HYDROCHLORIDE is hydrochlorothiazide; propranolol hydrochloride. There are thirty-one drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the hydrochlorothiazide; propranolol hydrochloride profile page.

Summary for NDA: 071972

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Therapeutic Class:Antimigraine Agents
Cardiovascular Agents
Formulation / Manufacturing:see details

Pharmacology for NDA: 071972

Mechanism of ActionAdrenergic beta-Antagonists

Suppliers and Packaging for NDA: 071972

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
PROPRANOLOL HYDROCHLORIDE
propranolol hydrochloride
TABLET;ORAL 071972 ANDA NCS HealthCare of KY, Inc dba Vangard Labs 0615-7761 0615-7761-39 30 TABLET in 1 BLISTER PACK (0615-7761-39)
PROPRANOLOL HYDROCHLORIDE
propranolol hydrochloride
TABLET;ORAL 071972 ANDA REMEDYREPACK INC. 24236-370 24236-370-02 30 TABLET in 1 BLISTER PACK (24236-370-02)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength10MG
Approval Date:Apr 6, 1988TE:ABRLD:No


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Serving leading biopharmaceutical companies globally:

Cerilliant
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Dow
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