Active Pharmaceutical Ingredient

Ramipril API Manufacturer & Supplier in India

Also known as: Altace; Tritace; Ramace

GMP Certified IP / BP / EP / USP ACE Inhibitor / Antihypertensive Aurangabad, India
Ramipril API Supplier Manufacturer Aurangabad Maharashtra India — Mediocon Inc
Ramipril IP / BP / EP / USP  |  GMP Certified  |  Mediocon Inc, Maharashtra, India
CAS No: 87333-19-5

Product Overview

Ramipril is an ACE inhibitor widely used for the treatment of hypertension, heart failure, and to reduce the risk of myocardial infarction, stroke, and cardiovascular death. Mediocon Inc manufactures GMP-compliant Ramipril at its Aurangabad facility to international pharmacopoeial standards.

Therapeutic Applications
  • Hypertension management
  • Heart failure treatment
  • Post-myocardial infarction cardiac protection
  • Diabetic nephropathy prevention
  • Cardiovascular risk reduction

Technical Specifications

ParameterSpecification
CAS Number87333-19-5
Molecular FormulaC₂₃H₃₂N₂O₅
Molecular Weight416.51 g/mol
GradeIP / BP / EP / USP
CategoryACE Inhibitor / Antihypertensive
AssayNLT 98.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
Residue on IgnitionNMT 0.1%
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
Batch NoRMP/24032026
Mfg DateMAR 2026
Exp DateFEB 2031
Packing25 kg HDPE drums / as per requirement

Quality & Compliance

  • GMP Certified manufacturing facility in Aurangabad, Maharashtra, India
  • Full pharmacopoeial compliance: IP / BP / EP / USP standards
  • Complete documentation: Certificate of Analysis (CoA), MSDS, Certificate of Origin
  • Stringent in-process quality control at every manufacturing stage
  • HPLC purity testing and spectroscopic identification (IR, NMR)
  • Cold-chain and controlled-environment storage facilities available
  • Exported to 40+ countries with full regulatory support

Sourcing, Regulatory & Export Information

Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Ramipril — CAS 87333-19-5 (CAS 87333-19-5) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Ramipril — CAS 87333-19-5 is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing — identity (IR/HPLC), assay, related substances, residual solvents (ICH Q3C), heavy metals, and microbial limits — before release with a Certificate of Analysis.

Export Markets

  • USA — FDA-registered facility; DMF support available for ANDA/NDA filings
  • Europe — EMA-compliant documentation; CEP/EDMF support on request
  • Africa & Middle East — WHO-GMP certified; competitive pricing for emerging markets
  • Southeast Asia — established logistics network; temperature-controlled shipments
  • India domestic — schedule H/X compliance; all state licensing documentation provided

Quality & Compliance

  • ISO 9001:2015 certified quality management system
  • GMP-certified manufacturing facility, Aurangabad, Maharashtra
  • Full batch traceability from raw material to finished API
  • Stability data available (ICH Q1A guidelines) for regulatory submissions
  • Dedicated QA team for customer audits and regulatory queries

Frequently Asked Questions — Ramipril — CAS 87333-19-5 API

What is the minimum order quantity for Ramipril — CAS 87333-19-5 API?
Mediocon Inc supplies Ramipril — CAS 87333-19-5 with a minimum order quantity of 1 kg (sample packs available for R&D). We accommodate both small R&D quantities and large commercial-scale orders. Contact our sales team at akshay@mediocon.com or +91 9309999757 for a tailored quote.
What pharmacopoeial grades of Ramipril — CAS 87333-19-5 does Mediocon supply?
We supply Ramipril — CAS 87333-19-5 conforming to IP / BP / EP / USP pharmacopoeial standards. Each batch is tested against full pharmacopoeial specifications and released with a Certificate of Analysis. Custom specifications can be accommodated for regulated markets.
What documentation is provided with Ramipril — CAS 87333-19-5 API?
Every shipment of Ramipril — CAS 87333-19-5 comes with: Certificate of Analysis (CoA), MSDS/SDS, Certificate of Origin (COO), and Drug Master File (DMF) support on request. We also provide GMP certification, ISO 9001:2015 compliance documentation, and full regulatory support for filings in USA (FDA), Europe (EMA), and other markets.
What is the lead time and shipping for Ramipril — CAS 87333-19-5 bulk orders?
Standard lead time for Ramipril — CAS 87333-19-5 is 2–4 weeks for standard orders; expedited shipments possible for urgent requirements. We ship to 40+ countries worldwide using approved pharmaceutical-grade packaging (25 kg HDPE drums / aluminium foil bags). All shipments include temperature-controlled logistics options where required by the product's storage conditions.
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