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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 217957
Company: UBI
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LEUPROLIDE ACETATE LEUPROLIDE ACETATE 14MG/2.8ML (1MG/0.2ML) SOLUTION;SUBCUTANEOUS Prescription AP No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
10/17/2024 ORIG-1 Approval STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
09/23/2025 SUPPL-2 Labeling-Package Insert, Labeling-Container/Carton Labels

Label is not available on this site.

LEUPROLIDE ACETATE

SOLUTION;SUBCUTANEOUS; 14MG/2.8ML (1MG/0.2ML)
TE Code = AP

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
LEUPROLIDE ACETATE LEUPROLIDE ACETATE 14MG/2.8ML (1MG/0.2ML) SOLUTION;SUBCUTANEOUS Prescription No AP 215336 AMNEAL
LEUPROLIDE ACETATE LEUPROLIDE ACETATE 14MG/2.8ML (1MG/0.2ML) SOLUTION;SUBCUTANEOUS Prescription No AP 212963 EUGIA PHARMA
LEUPROLIDE ACETATE LEUPROLIDE ACETATE 14MG/2.8ML (1MG/0.2ML) SOLUTION;SUBCUTANEOUS Prescription No AP 075471 MEITHEAL
LEUPROLIDE ACETATE LEUPROLIDE ACETATE 14MG/2.8ML (1MG/0.2ML) SOLUTION;SUBCUTANEOUS Prescription No AP 074728 SANDOZ
LEUPROLIDE ACETATE LEUPROLIDE ACETATE 14MG/2.8ML (1MG/0.2ML) SOLUTION;SUBCUTANEOUS Prescription No AP 213829 SOMERSET THERAPS LLC
LEUPROLIDE ACETATE LEUPROLIDE ACETATE 14MG/2.8ML (1MG/0.2ML) SOLUTION;SUBCUTANEOUS Prescription No AP 078885 SUN PHARM
LEUPROLIDE ACETATE LEUPROLIDE ACETATE 14MG/2.8ML (1MG/0.2ML) SOLUTION;SUBCUTANEOUS Prescription No AP 217957 UBI
LEUPROLIDE ACETATE LEUPROLIDE ACETATE 14MG/2.8ML (1MG/0.2ML) SOLUTION;SUBCUTANEOUS Prescription No AP 215826 ZYDUS PHARMS
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