Overview

Pharmaceutical manufacturing site surfaced via EU GMP non-compliance screening (EudraGMDP).

Core services & business areas

API Manufacturing

Active pharmaceutical ingredients supplied

Substances MEHTA API Pvt. Ltd. is evidenced to supply (US FDA Drug Master File or EU CEP). Open any ingredient to see its full supplier landscape, CAS number and patent status.

API / Drug Master Files

MEHTA API Pvt. Ltd. holds 8 active (8 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.

  • VISMODEGIB IHActive2026-03-16
  • AGOMELATINE IHActive2026-02-03
  • CINACALCET HYDROCHLORIDE IHActive2025-12-08
  • DROPERIDOL USPActive2025-07-02
  • LANDIOLOL HYDROCHLORIDEActive2025-01-29
  • MIRABEGRON EPActive2024-10-18
  • CARIPRAZINE HYDROCHLORIDE IHActive2024-09-12
  • ESMOLOL HCL USPActive2024-01-31

FDA compliance signals

1 FDA enforcement record linked to this company.

  • eu_noncompliance2019-11-25

    EU GMP Statement of Non-Compliance

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