| Contacts: | Gayane Margaryan, MD, BS, CPhT |
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Resource Conservation and Recovery Act (RCRA) Laws and Regulations
RCRA gives U.S. Environmental Protection Agency (EPA) the authority to control hazardous waste the generation, transportation, storage and disposal of hazardous waste. To achieve this, EPA develops regulations, guidance and policies. RCRA Online is an electronic database that indexes thousands of letters, memoranda, publications, and questions and answers issued by EPA. These documents include EPA interpretations of the RCRA regulations governing the management of solid, hazardous, and medical waste. Who Regulates Medical Waste? Medical waste is primarily regulated by state environmental and health departments. EPA has not had authority, specifically for medical waste, since the Medical Waste Tracking Act (MWTA) of 1988 expired in 1991. It is important to contact your state environmental program first when disposing of medical waste. Contact your state environmental protection agency and your state health agency for more information regarding your state's regulations on medical waste. Other federal agencies have regulations regarding medical waste. These agencies include Centers for Disease Control (CDC), Occupational Safety and Health Administration (OSHA), U.S. Food and Drug Administration (FDA), and potentially others. Learn how to dispose of unused or expired drugs The U.S. Drug Enforcement Administration (DEA) sponsors National Prescription Drug Take Back Day in communities nationwide. Many communities also have their own drug take back programs. Find a DEA-authorized collector in your community. List of medicines, recommended by FDA for disposal by flushing. For complete details and instructions on safe medicine disposal, visit www.FDA.Gov/DrugDisposal.
United States Pharmacopeia (USP) All Products Compounding standards USP 795 "Nonsterile" | 797 "Sterile" | 800 "Hazardous" | 825 "Radiopharmaceuticals" USP Compounding Standards and Beyond-Use Dates Reference Standards Catalog currently offers more than 3,500 Reference Standards—highly characterized specimens of drug substances, excipients, food ingredients, impurities, degradation products, dietary supplements Download as PDF as Excel as CSV GoodRx
U.S. Food & Drug Administration (FDA)
Institute for Safe Medication Practices (ISMP) FDA-Approved Drugs Browse by Drug Name A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9 FDA Recommended to Use Tall Man Lettering (TML) for some Drug Names FDA Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations The Orange Book facilitates market access for generic drugs by establishing their therapeutic equivalence to brand-name drugs. FDA National Drug Code Directory Each listed drug product is assigned a unique 10-digit, 3-segment number. This number, known as the NDC, identifies the labeler, product, and trade package size. FDA Purple Book: Database of Licensed Biological Products Download Purple Book Data The Purple Book helps biologic/biosimilar product manufacturers understand if a biological product has been approved by the FDA. Purple Book does not include synthetic products. It lists biological products, also known as biologics or large-molecule drugs. These include therapeutic proteins, allergenic products, cellular and gene therapies, and vaccines. The Purple Book includes information about Innovator biological products, Biosimilar and interchangeable biological products, Reference product exclusivity. Online Search in Purple Book Database . Online Voluntary Reporting Forms. FDA MedWatch alerts for Human Medical Products (Drugs, Biologics, Medical Devices, Special Nutritional Products and Cosmetics). Reporting can be done also by completing and then submitting FDA Form 3500 (health professional) or 3500B (consumer/patient). FDA Adverse Event Reporting System FAERS represent the reported information. FAERS data by themselves are not an indicator of the safety profile of the drug or biologic. While consumers and healthcare professionals are encouraged to report adverse events, the incident could have been caused by the underlying disease being treated, another drug being used concurrently, or for other reasons. Certain data fields, such as a narrative description of the adverse event, are not publicly available to protect patient privacy. Healthcare Practitioner’s Error Reporting Forms for Medication ISMP MERP and Vaccine ISMP VERP . While both "ISMP MERP" and "MedWatch" are systems for reporting medication-related safety concerns, ISMP MERP specifically focuses on medication errors across the entire medication use process (prescribing, dispensing, administration) and is primarily managed by the Institute for Safe Medication Practices (ISMP), whereas MedWatch is a broader FDA program for reporting adverse events related to any medical product, including drugs. ISMP Consumers Report VAERS Vaccine Adverse Event Reporting System. is co-sponsored by the Centers for Disease Control and Prevention (CDC), and the Food and Drug Administration (FDA), agencies of the U.S. Department of Health and Human Services (HHS). ISMP List of High-Alert Medications: Acute Care Settings 2024 | Community/Ambulatory Healthcare 2017 | Long-Term Care (LTC) Settings 2017 FDA REMS Risk Evaluation and Mitigation Strategies FDA Medication Guides FDA Drug Recalls Wholesale Drug Distributors Database of FDA Each line of this reporting database represents a license for a particular facility. One facility may have multiple licenses and therefore multiple lines may be listed in the database. This database is updated every business day. Explore over hundreds of CE Courses for Pharmacists and Pharmacy Technicians CFR Resources:GPO Electronic Code of Federal Regulations (eCFR)Most up-to-date version of CFR Title 21 Currently updated online version Controlled Substances MeSHRUS и LOINC 2020
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| Medium Pharmaceutical 211 212 213 214 215 216 217 218 219 221 222 223 224 225 226 227 228 229 24x26 28x26 23x29 25x21 22x28 30x26 28x34 |
Small Pharmaceutical 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 201 202 203 204 205 206 207 208 209 191 192 193 194 |
| Large Pharmaceutical 1 1-1 1-2 65-25 25-65 2 3 4 5 6 7 8 9 10 36x34 32x32 33x36 34x36 35x35 36x33 32x22 30x24 30x30 |
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Arm-Latin crossword "direction" Arm-Latin...anatomy 3 ... 4 Rus-Latin...anatomy 1 ... 2 ... 3 | |