FDA Orange Book

Generic for Xylocaine Viscous

Xylocaine Viscous contains lidocaine. 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 Xylocaine Viscous is lidocaine. 7 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AT.

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Xylocaine Viscous products in the Orange Book

Xylocaine Viscous products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
solution, oral2%DiscontinuedNone7AT

NDA 009470, held by FRESENIUS KABI USA LLC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic lidocaine

Approved generic versions of Xylocaine Viscous
CompanyANDATE codeApprovedStrengths
PHARMOBEDIENT CONSULTING LLC087872AT (A-rated, therapeutically equivalent)November 18, 19822%
HIKMA PHARMACEUTICALS USA INC088802AT (A-rated, therapeutically equivalent)April 26, 19852%
CHARTWELL MOLECULAR HOLDINGS LLC040708AT (A-rated, therapeutically equivalent)February 27, 20072%
RUBICON RESEARCH LTD216780AT (A-rated, therapeutically equivalent)March 28, 20232%
PAI HOLDINGS LLC DBA PHARMACEUTICAL ASSOCIATES INC218138AT (A-rated, therapeutically equivalent)February 20, 20242%
AUROBINDO PHARMA LTD219759AT (A-rated, therapeutically equivalent)July 29, 20252%
QUAGEN PHARMACEUTICALS LLC218676AT (A-rated, therapeutically equivalent)March 20, 20262%

Questions

Is there a generic for Xylocaine Viscous?

Yes. The generic name for Xylocaine Viscous is lidocaine. 7 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AT.

What is the generic name for Xylocaine Viscous?

The active ingredient in Xylocaine Viscous is lidocaine, 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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