FDA Orange Book

Is there a generic for Konvomep?

Konvomep contains omeprazole and sodium bicarbonate. 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 Konvomep (omeprazole and sodium bicarbonate). The Orange Book shows its last listed patent expires March 1, 2040.

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Konvomep products in the Orange Book

Konvomep products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
for suspension, oral2MG/ML;84MG/MLMarketed (Rx)None0None

NDA 213593, held by AZURITY PHARMACEUTICALS INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Konvomep patents

Patents listed for Konvomep
PatentExpiresCoversUse codeNDA
11911473July 16, 2039Method of useU-623213593
11911473July 16, 2039Method of useU-624213593
12440566July 16, 2039Drug productNone213593
12329752July 16, 2039Drug productNone213593
10751333July 16, 2039Drug productNone213593
11103492July 16, 2039Drug productNone213593
11633478July 16, 2039Drug productNone213593
12042539July 16, 2039Drug productNone213593
11771686March 1, 2040Method of useU-623213593

Questions

Is there a generic for Konvomep?

No. The Orange Book lists no active FDA-approved generic (ANDA) for Konvomep (omeprazole and sodium bicarbonate). The Orange Book shows its last listed patent expires March 1, 2040.

What is the generic name for Konvomep?

The active ingredient in Konvomep is omeprazole and sodium bicarbonate, per the FDA Orange Book.

When does the Konvomep patent expire?

The last patent listed for Konvomep in the Orange Book expires March 1, 2040. 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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