Active Pharmaceutical Ingredient

Medroxy Progesterone Acetate

Also known as: MPA; Depo-Provera; Provera

CAS: 71-58-9 Progestogen IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Medroxy Progesterone Acetate API — Mediocon Inc
Medroxy Progesterone Acetate — Pharmaceutical Grade API | Mediocon Inc, Aurangabad, Maharashtra, India

Product Overview

CAS No: 71-58-9  |  MF: C₂₄H₃₄O₄  |  MW: 386.52 g/mol

Medroxy Progesterone Acetate is a high-purity Progestogen supplied by Mediocon Inc as an Active Pharmaceutical Ingredient (API) conforming to IP / BP / EP / USP specifications. Manufactured at our GMP-certified facility in Aurangabad, Maharashtra, India, it meets the stringent quality requirements of global pharmaceutical manufacturers.

Medroxy Progesterone Acetate (MPA) is a widely used synthetic progestogen available in oral and injectable forms. It is used for contraception, hormone replacement therapy, treatment of endometriosis, and management of certain cancers.

Key Features

  • High-purity pharmaceutical grade API
  • IP / BP / EP / USP compliant
  • Full CoA and MSDS documentation
  • GMP certified manufacturing facility

Applications

  • Injectable contraception (Depo-Provera)
  • Hormone replacement therapy
  • Treatment of endometriosis
  • Management of endometrial and renal cell carcinoma

Why Choose Mediocon

  • ISO 9001:2015 & GMP certified manufacturing
  • Consistent batch-to-batch quality with full CoA
  • Export-ready documentation: COO, MSDS, DMF
  • Flexible MOQ for both R&D and commercial scale
  • Dedicated QA support for regulatory filings

Product Specifications

Product NameMedroxy Progesterone Acetate
Also Known AsMPA; Depo-Provera; Provera
CAS Number71-58-9
Molecular FormulaC₂₄H₃₄O₄
Molecular Weight386.52 g/mol
CategoryProgestogen
AppearanceWhite to off-white crystalline powder
SolubilityPractically insoluble in water; soluble in ethanol, chloroform
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
AssayNLT 98.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
Residue on IgnitionNMT 0.1%
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
Packing25 kg HDPE drums / as per requirement
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