FDA Orange Book

Generic for VePesid

VePesid contains etoposide. Orange Book status for every listed strength, the approved generic makers, and the listed patents and exclusivities.

Source: FDA Orange Book data file dated 2026-10-09. Publisher page

Yes. The generic name for VePesid is etoposide. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB, AP. Generics match 2 of the 3 VePesid products the Orange Book lists.

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VePesid products in the Orange Book

VePesid products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
capsule, oral100MGDiscontinuedNone0None
capsule, oral50MGMarketed (Rx)AB1AB
injectable, injection20MG/MLDiscontinuedNone4AP

NDA 019557, 018768, held by ONESOURCE SPECIALTY PTE LTD. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic etoposide

Approved generic versions of VePesid
CompanyANDATE codeApprovedStrengths
HIKMA PHARMACEUTICALS USA INC074290AP (A-rated, therapeutically equivalent)July 17, 199520MG/ML
ACCORD HEALTHCARE INC074513AP (A-rated, therapeutically equivalent)March 14, 199620MG/ML
MEITHEAL PHARMACEUTICALS INC074529AP (A-rated, therapeutically equivalent)July 24, 199620MG/ML
FRESENIUS KABI USA LLC074983AP (A-rated, therapeutically equivalent)September 30, 199820MG/ML
MYLAN PHARMACEUTICALS INC075635AB (A-rated, therapeutically equivalent)September 19, 200150MG

VePesid NDC codes

Questions

Is there a generic for VePesid?

Yes. The generic name for VePesid is etoposide. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB, AP. Generics match 2 of the 3 VePesid products the Orange Book lists.

What is the generic name for VePesid?

The active ingredient in VePesid is etoposide, per the FDA Orange Book.

What does a therapeutic equivalence code mean?

In the Orange Book, codes that start with A (such as AB) mean FDA considers the product therapeutically equivalent to the reference drug. Codes that start with B mean FDA does not, at this time, consider the product therapeutically equivalent.

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