FDA Orange Book

Is there a generic for Contepo?

Contepo contains fosfomycin. 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

No. The Orange Book lists no active FDA-approved generic (ANDA) for Contepo (fosfomycin). The Orange Book shows its last listed patent expires January 30, 2039 and its last listed exclusivity ends October 22, 2033.

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Contepo products in the Orange Book

Contepo products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
powder, intravenousEQ 6GM BASE/VIALMarketed (Rx)None0None

NDA 212271, held by MEITHEAL PHARMACEUTICALS INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Contepo patents

Patents listed for Contepo
PatentExpiresCoversUse codeNDA
10086006October 12, 2034Method of useU-4332212271
9345717October 27, 2034Method of useU-4332212271
11541064January 30, 2039Method of useU-4331212271
12702676January 30, 2039Method of useU-4331212271

Contepo exclusivity

Exclusivity listed for Contepo
CodeMeaningExpiresNDA
NPNew productOctober 22, 2028212271
GAINGenerating Antibiotic Incentives NowOctober 22, 2033212271

Contepo NDC codes

Questions

Is there a generic for Contepo?

No. The Orange Book lists no active FDA-approved generic (ANDA) for Contepo (fosfomycin). The Orange Book shows its last listed patent expires January 30, 2039 and its last listed exclusivity ends October 22, 2033.

What is the generic name for Contepo?

The active ingredient in Contepo is fosfomycin, per the FDA Orange Book.

When does the Contepo patent expire?

The last patent listed for Contepo in the Orange Book expires January 30, 2039. A listed patent expiry date is not a generic launch date.

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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