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Re: None

Wednesday, 03/13/2019 4:00:14 PM

Wednesday, March 13, 2019 4:00:14 PM

Post# of 187
$TLGT FDA Approval of Desonide topical ointment?!?

https://www.accessdata.fda.gov/scripts/cder/ob/results_product.cfm?Appl_Type=A&Appl_No=212002

Product Details for ANDA 212002
DESONIDE (DESONIDE)
0.05% Marketing Status: Prescription
Active Ingredient: DESONIDE
Proprietary Name: DESONIDE
Dosage Form; Route of Administration: OINTMENT; TOPICAL
Strength: 0.05%
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A212002
Product Number: 001
Approval Date: Mar 12, 2019
Applicant Holder Full Name: TELIGENT PHARMA INC
Marketing Status: Prescription
Patent and Exclusivity Information



GLTA!!

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