Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 206772

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DOXYCYCLINE HYCLATE (DOXYCYCLINE HYCLATE)
EQ 75MG BASE
Marketing Status: Discontinued

Active Ingredient: DOXYCYCLINE HYCLATE
Proprietary Name: DOXYCYCLINE HYCLATE
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A206772
Product Number: 001
Approval Date: Dec 21, 2018
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

DOXYCYCLINE HYCLATE (DOXYCYCLINE HYCLATE)
EQ 100MG BASE
Marketing Status: Discontinued

Active Ingredient: DOXYCYCLINE HYCLATE
Proprietary Name: DOXYCYCLINE HYCLATE
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 100MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A206772
Product Number: 002
Approval Date: Dec 21, 2018
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

DOXYCYCLINE HYCLATE (DOXYCYCLINE HYCLATE)
EQ 150MG BASE
Marketing Status: Discontinued

Active Ingredient: DOXYCYCLINE HYCLATE
Proprietary Name: DOXYCYCLINE HYCLATE
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 150MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A206772
Product Number: 003
Approval Date: Dec 21, 2018
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information