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USP Certificate Related Compound C LOT F0L067 Molecular Formula C10H12Cl2N2 . HCl Molecular Weight 267.58 CAS Number 119532262 LABEL TEXT Quality Assurance Page 1 of 2 9Mar12 Calculation.

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USP is a scientific nonprofit organization that sets public standards for identity, strength, quality and purity of medicines. USP standards are recognized in various provisions of the federal Food, Drug and Cosmetic Act (FDCA) and in laws, regulations and policies promulgated by states.

Where can I find the USP Certificate for a USP Reference Standard? USP Certificates for current & previous lots, when available, can be viewed on our website by clicking on the Product Description of the RS in the online USP store.

The USP Certificate of Document and Reference Standards provides prospect with the knowledge of the effective use of USP standards in the Pharmaceutical industry for the development and manufacture of medicines.

All available USP Reference Standards (RS) can be purchased in the USP iStore . You can sign up to be notified when anew never-before-released Reference Standard becomes available through the Reference Standards Release Notification Program .

The most trusted Reference Standards USP currently offers more than 3,500 Reference Standards—highly characterized specimens of drug substances, excipients, food ingredients, impurities, degradation products, dietary supplements, compendial reagents and performance calibrators.

USP Reference Standards are substances selected for their high purity, critical characteristics, and suitability for the intended purpose. Heterogeneous substances, of natural origin, also are designated “Reference Standards” where needed. Usually these are the counterparts of international standards.

USP develops and publishes standards for drug substances, drug products, excipients, and dietary supplements in the United States Pharmacopeia–National Formulary (USP–NF). These standards have been recognized in the Federal Food, Drug and Cosmetic (FD&C) Act since it was first enacted in 1938.

The reference standard should be of the highest purity possible; the drug substance may require further purification to become a reference standard (additional purification steps used for a drug substance should be fully described and included in any regulatory filing).

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© Copyright 1997-2025
airSlate Legal Forms, Inc.
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Form Packages
Adoption
Bankruptcy
Contractors
Divorce
Home Sales
Employment
Identity Theft
Incorporation
Landlord Tenant
Living Trust
Name Change
Personal Planning
Small Business
Wills & Estates
Packages A-Z
Form Categories
Affidavits
Bankruptcy
Bill of Sale
Corporate - LLC
Divorce
Employment
Identity Theft
Internet Technology
Landlord Tenant
Living Wills
Name Change
Power of Attorney
Real Estate
Small Estates
Wills
All Forms
Forms A-Z
Form Library
Customer Service
Terms of Service
DMCA Policy
About Us
Blog
Affiliates
Contact Us
Privacy Notice
Delete My Account
Site Map
All Forms
Search all Forms
Industries
Forms in Spanish
Localized Forms
Legal Guides
Real Estate Handbook
All Guides
Prepared for You
Notarize
Incorporation services
Our Customers
For Consumers
For Small Business
For Attorneys
Our Sites
US Legal Forms
USLegal
FormsPass
pdfFiller
signNow
airSlate workflows
DocHub
Instapage
Social Media
Call us now toll free:
1-877-389-0141
As seen in:
  • USA Today logo picture
  • CBC News logo picture
  • LA Times logo picture
  • The Washington Post logo picture
  • AP logo picture
  • Forbes logo picture
© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232