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FDA Approval

Vilevev MB

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Vilvet Pharmaceuticals Inc
DUNS: 080444356
Effective Date
February 21, 2019
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Vilevev MB

Product Details

NDC Product Code
71186-000
Route of Administration
ORAL
Effective Date
February 21, 2019
Code: 28A37T47QOClass: ACTIBQuantity: 32.4 mg in 1 1
Code: J50OIX95QVClass: ACTIBQuantity: 81 mg in 1 1
Code: 8NAP7826UBClass: ACTIRQuantity: 10.8 mg in 1 1
Code: F2R8V82B84Class: ACTIBQuantity: 0.12 mg in 1 1
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