Skip to main content Skip to search Skip to main navigation
News: International

India: Restricted exports of APIs due to coronavirus

As the Indian Directorate General of Foreign Trade announced on 3 March 2020, the export of 26 active ingredients and medicinal products will be severely restricted until further notice due to the global spread of the coronavirus.

There is no further explanation from the government. Dinesh Dua, chairman of the Pharmaceuticals Export Promotion Council of India, told Reuters that acute shortages could occur in the next months if the virus-related disruptions in production and supply chains continue. A large proportion of the low-cost generic pharmaceuticals come from India. The country receives about 70 percent of its active ingredients and medicinal products from China and further processes a large part of them for export.

The supply of the following Indian active ingredients and medicinal products, as well as formulations thereof, is now restricted:

  • Aciclovir
  • Chloramphenicol
  • Clindamycin
  • Erythromycin
  • Metronidazole
  • Neomycin
  • Ornidazole
  • Paracetamol
  • Progesterone
  • Tinidazole
  • Vitamin B1 (thiamine)
  • Vitamin B6 (pyridoxine)
  • Vitamin B12 (cobalamin)

Fierce Pharma: Coronavirus spurs India to restrict exports of 2 dozen drugs

DAZ Online: India stops drug exports - which drugs could become scarce?

 

Meet the GMP Compliance Adviser

The GMP Compliance Adviser is the world's largest knowledge portal for quality management in the pharma business. 

The demo access is non-binding and ends automatically.

Test it now for free

You may also be interested in the following articles:

News: EMA

EMA Clarifies Batch Numbering for Parallel-Traded Medicines

EMA updated its GMP/GDP Q&A collection by revising the answer to Question 4 concerning Chapter 5 of the EU GMP Guide. It explains which batch numbers should appear on the packaging of parallel-traded medicines.

Read more
Cleaning Validation: When PDE Reports and the Worst-Case Selection do not Align

Cleaning Validation: When PDE Reports and the Worst-Case Selection do not Align

Robust PDE reports form the basis of risk-based cleaning validation. This article highlights common deficiencies identified during GMP inspections and explains how they can be avoided.

Read more
Question of the Week | GMP-Verlag

Why is it Important to use Consistent Microbiological Air Monitoring Methods in Pharmaceutical Cleanrooms?

Here's the answer:
Read more
News: Europe

EDQM: New Working Party on 3D-printed Medicinal Products

The European Pharmacopoeia Commission (EPC) approved the creation of a working party on 3D-printed medicinal products. Its aim is to support the development of appropriate quality standards in the European Pharmacopoeia (Ph. Eur.).
Read more
EMA: 14 New Nitrosamines for Appendix 1

EMA: 14 New Nitrosamines for Appendix 1

Appendix 1 of EMA’s Questions and Answers on nitrosamine impurities has been updated. This appendix contains acceptable intakes (AIs) established for N-nitrosamines.
Read more
WHO: Draft Revision of its Guidelines on Quality Risk Management

WHO: Draft Revision of its Guidelines on Quality Risk Management

WHO published a revised draft of its “WHO guidelines on quality risk management”. Working document QAS/26.994 is open for public comment until 15 November 2026.
Read more
Previous
Next