Holds one active US DMF for acyclovir, filing since 2011. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 10 markets.
Holds 2 active US DMFs for acyclovir, filing since 2011. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds one active US DMF for acyclovir, filing since 2010. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for acyclovir, filing since 2025. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Its GMP is recognised in 1 market.
Holds one active US DMF for acyclovir, filing since 1998. Its 2025 FDA inspection closed as VAI.
Holds one active US DMF for acyclovir, filing since 2024. Its GMP is recognised in 1 market.
Holds one active US DMF for acyclovir, filing since 2025. Its GMP is recognised in 1 market.
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 Acyclovir 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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