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Serving hundreds of leading biopharmaceutical companies globally:

Colorcon
Johnson and Johnson
Fuji
Cipla
Queensland Health
Covington
Citi
Mallinckrodt
Julphar

Generated: April 26, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 012772

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NDA 012772 describes HALDRONE, which is a drug marketed by Lilly and is included in one NDA. Additional details are available on the HALDRONE profile page.

The generic ingredient in HALDRONE is paramethasone acetate. There are two drug master file entries for this compound. Additional details are available on the paramethasone acetate profile page.
Summary for 012772
Tradename:HALDRONE
Applicant:Lilly
Ingredient:paramethasone acetate
Patents:0
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 012772

Profile for product number 005

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength1MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

Profile for product number 006

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength2MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

Expired US Patents for NDA 012772

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Lilly HALDRONE paramethasone acetate TABLET;ORAL 012772-005 Approved Prior to Jan 1, 1982 ➤ Sign Up ➤ Sign Up
Lilly HALDRONE paramethasone acetate TABLET;ORAL 012772-006 Approved Prior to Jan 1, 1982 ➤ Sign Up ➤ Sign Up
Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration

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Serving hundreds of leading biopharmaceutical companies globally:

Cerilliant
Chinese Patent Office
Fish and Richardson
Farmers Insurance
McKesson
Healthtrust
Chubb
Cantor Fitzgerald
US Army

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