Holds one active US DMF for prucalopride, filing since 2023. Its 2026 FDA inspection closed as NAI, and its GMP is recognised in 20 markets.
Holds one active US DMF for prucalopride, filing since 2023. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds one active US DMF for prucalopride, filing since 2022. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 26 markets.
Holds 2 active US DMFs for prucalopride, filing since 2020. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for prucalopride, filing since 2020. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds one active US DMF for prucalopride, filing since 2022. Its 2024 FDA inspection closed as NAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for prucalopride, filing since 2025. Its 2025 FDA inspection closed as VAI.
Holds 2 active US DMFs for prucalopride, filing since 2024.
Registered with SFDA (Saudi Arabia) for prucalopride. Its GMP is recognised in 2 markets.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
This page filters the worldwide Prucalopride manufacturer list to companies based in India. The order is set by active filings weighted by regulator, inspection outcomes and their recency, breadth of GMP recognition, and evidence of real exports, less any open risk flags. Read the full method.
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