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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 065389

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DEMECLOCYCLINE HYDROCHLORIDE (DEMECLOCYCLINE HYDROCHLORIDE)
150MG
Marketing Status: Prescription
Active Ingredient: DEMECLOCYCLINE HYDROCHLORIDE
Proprietary Name: DEMECLOCYCLINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A065389
Product Number: 001
Approval Date: Dec 1, 2008
Applicant Holder Full Name: EPIC PHARMA LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
DEMECLOCYCLINE HYDROCHLORIDE (DEMECLOCYCLINE HYDROCHLORIDE)
300MG
Marketing Status: Prescription
Active Ingredient: DEMECLOCYCLINE HYDROCHLORIDE
Proprietary Name: DEMECLOCYCLINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A065389
Product Number: 002
Approval Date: Dec 1, 2008
Applicant Holder Full Name: EPIC PHARMA LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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