FDA Orange Book

Generic for Parafon Forte Dsc

Parafon Forte Dsc contains chlorzoxazone. 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 Parafon Forte Dsc is chlorzoxazone. 7 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AA.

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Parafon Forte Dsc products in the Orange Book

Parafon Forte Dsc products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
tablet, oral500MGDiscontinuedNone7AA

NDA 011529, held by JANSSEN RESEARCH AND DEVELOPMENT LLC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic chlorzoxazone

Approved generic versions of Parafon Forte Dsc
CompanyANDATE codeApprovedStrengths
AUROBINDO PHARMA LTD089853AA (A-rated, therapeutically equivalent)May 4, 1988500MG
WATSON LABORATORIES INC089859AA (A-rated, therapeutically equivalent)May 4, 1988500MG
NOVITIUM PHARMA LLC212254AA (A-rated, therapeutically equivalent)September 12, 2019500MG
DR REDDYS LABORATORIES SA211849AA (A-rated, therapeutically equivalent)July 21, 2020500MG
RISING PHARMA HOLDINGS INC213126AA (A-rated, therapeutically equivalent)April 5, 2022500MG
MACLEODS PHARMACEUTICALS LTD214941AA (A-rated, therapeutically equivalent)October 20, 2022500MG
PHARMAZONE210961AA (A-rated, therapeutically equivalent)January 22, 2024500MG

Questions

Is there a generic for Parafon Forte Dsc?

Yes. The generic name for Parafon Forte Dsc is chlorzoxazone. 7 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AA.

What is the generic name for Parafon Forte Dsc?

The active ingredient in Parafon Forte Dsc is chlorzoxazone, 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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