Navesta Pharmaceuticals (Pvt) Ltd.
Overview
Pharmaceutical manufacturing site surfaced via EU GMP non-compliance screening (EudraGMDP).
API / Drug Master Files
Navesta Pharmaceuticals (Pvt) Ltd. holds 3 active (4 total) FDA Type II Drug Master Files — identifying it as an active-substance / API supplier. Type II DMFs are filed with the FDA to support the use of an active pharmaceutical ingredient in drug applications.
- POVIDONE-IODINE USPActive2019-04-02
- VIGABATRINActive2018-09-22
- OXYTOCINActive2012-09-22
- OCTREOTIDE ACETATEInactive2012-06-13
FDA compliance signals
1 FDA enforcement record linked to this company.
- eu_noncompliance2026-05-11
EU GMP Statement of Non-Compliance
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