Leuprolide Acetate
Leuprolide Acetate Injection Rx only
Approved
Approval ID
bec9077a-3f04-4887-856d-dde2de24584d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 25, 2023
Manufacturers
FDA
VGYAAN Pharmaceuticals LLC
DUNS: 024755855
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Leuprolide Acetate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72664-611
Application NumberANDA213829
Product Classification
M
Marketing Category
C73584
G
Generic Name
Leuprolide Acetate
Product Specifications
Effective DateSeptember 25, 2023
FDA Product Classification