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Generated: April 20, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 019137

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NDA 019137 describes BETAMETHASONE DIPROPIONATE, which is a drug marketed by Fougera Pharms, Glenmark Generics, Perrigo New York, Taro, Tolmar, Actavis Mid Atlantic, Pharmaderm, Teva, Teligent Pharma Inc, Alpharma Us Pharms, Fougera Pharms Inc, G And W Labs Inc, and Hi-tech Pharmacal, and is included in thirty-eight NDAs. It is available from sixteen suppliers. Additional details are available on the BETAMETHASONE DIPROPIONATE profile page.

The generic ingredient in BETAMETHASONE DIPROPIONATE is betamethasone dipropionate. There are sixty-six drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the betamethasone dipropionate profile page.
Summary for 019137
Tradename:BETAMETHASONE DIPROPIONATE
Applicant:Fougera Pharms
Ingredient:betamethasone dipropionate
Patents:0
Therapeutic Class:Hormonal Agents, Stimulant/Replacement/Modifying (Adrenal)
Formulation / Manufacturing:see details
Pharmacology for NDA: 019137
Suppliers and Packaging for NDA: 019137
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
BETAMETHASONE DIPROPIONATE betamethasone dipropionate CREAM;TOPICAL 019137 NDA E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. 0168-0055 N 0168-0055-15
BETAMETHASONE DIPROPIONATE betamethasone dipropionate CREAM;TOPICAL 019137 NDA E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. 0168-0055 N 0168-0055-46

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:CREAM;TOPICALStrengthEQ 0.05% BASE
Approval Date:Jun 26, 1984TE:ABRLD:Yes

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