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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 070929

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TAMOXIFEN CITRATE (TAMOXIFEN CITRATE)
EQ 10MG BASE
Marketing Status: Prescription
Active Ingredient: TAMOXIFEN CITRATE
Proprietary Name: TAMOXIFEN CITRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A070929
Product Number: 001
Approval Date: Feb 20, 2003
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status:  Prescription
Patent and Exclusivity Information
TAMOXIFEN CITRATE (TAMOXIFEN CITRATE)
EQ 20MG BASE
Marketing Status: Prescription
Active Ingredient: TAMOXIFEN CITRATE
Proprietary Name: TAMOXIFEN CITRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A070929
Product Number: 002
Approval Date: Feb 20, 2003
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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