Product Details for ANDA 065470
MINOCYCLINE HYDROCHLORIDE (MINOCYCLINE HYDROCHLORIDE)
EQ 50MG BASE
Marketing Status: Prescription
EQ 75MG BASE
Marketing Status: Prescription
EQ 100MG BASE
Marketing Status: Prescription
EQ 50MG BASE
Marketing Status: Prescription
Active Ingredient: MINOCYCLINE HYDROCHLORIDE
Proprietary Name: MINOCYCLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 50MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A065470
Product Number: 001
Approval Date: Mar 11, 2008
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Prescription
Patent and Exclusivity Information
MINOCYCLINE HYDROCHLORIDE (MINOCYCLINE HYDROCHLORIDE)
Proprietary Name: MINOCYCLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 50MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A065470
Product Number: 001
Approval Date: Mar 11, 2008
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Prescription
Patent and Exclusivity Information
EQ 75MG BASE
Marketing Status: Prescription
Active Ingredient: MINOCYCLINE HYDROCHLORIDE
Proprietary Name: MINOCYCLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A065470
Product Number: 002
Approval Date: Mar 11, 2008
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Prescription
Patent and Exclusivity Information
MINOCYCLINE HYDROCHLORIDE (MINOCYCLINE HYDROCHLORIDE)
Proprietary Name: MINOCYCLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A065470
Product Number: 002
Approval Date: Mar 11, 2008
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Prescription
Patent and Exclusivity Information
EQ 100MG BASE
Marketing Status: Prescription
Active Ingredient: MINOCYCLINE HYDROCHLORIDE
Proprietary Name: MINOCYCLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 100MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A065470
Product Number: 003
Approval Date: Mar 11, 2008
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: MINOCYCLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 100MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A065470
Product Number: 003
Approval Date: Mar 11, 2008
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status: Prescription
Patent and Exclusivity Information