Injectables Sample Clauses

Injectables d. All of the above
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Injectables. Off label use, unless approved by Us or the PBM or when the drug has been recognized as safe and effective for treatment of that indication in one or more of the standard medical reference compendia adopted by the United States Department of Health and Human Services or in medical literature that meets certain criteria. Medical literature may be accepted only if all of the following apply: (1) Two articles from major peer-reviewed professional medical journals have recognized the drug’s safety and effectiveness for treatment of the indication for which it has been prescribed; (2) No article from a major peer-reviewed professional medical journal has concluded that the drug is unsafe or ineffective or that the drug’s safety and effectiveness cannot be determined for the treatment of the indication for which it has been prescribed; (3) Each article meets the uniform requirements for manuscripts submitted to biomedical journals established by the international committee of medical journal editors or is published in a journal specified by the United States Department of Health and Human Services as acceptable peer-reviewed medical literature. Non covered Prescription Drug Benefits include: • Prescription Drugs dispensed by any Mail Service program other than Our Pharmacy Benefit Manager’s Mail Service, unless prohibited by law. • Drugs, devices and products, or Prescription Legend Drugs with over the counter equivalents and any Drugs, devices or products that are therapeutically comparable to an over the counter Drug, device, or product. This Exclusion does not apply to over-the-counter products that We must cover under federal law with a Prescription. • Drugs in quantities exceeding the quantity prescribed, or for any refill dispensed later than one year after the date of the original Prescription Order. • Drugs not approved by the FDA. • Charges for the administration of any Drug. • Drugs consumed at the time and place where dispensed or where the Prescription Order is issued, including but not limited to samples provided by a Physician. This does not apply to Drugs used in conjunction with a Diagnostic Service, with Chemotherapy performed in the office or Drugs eligible for coverage under the Medical Supplies benefit; they are Covered Services. • Any Drug which is primarily for weight loss. • Drugs not requiring a prescription by federal law (including Drugs requiring a prescription by state law, but not by federal law), except for injectable insulin. • Dru...
Injectables. Xylocaine 1% x 2 vials Xylocaine 1% Rid x 1 vial Celeston Solution x 1½ vials Kenalog 40mg x 1 vial Depo Medral 40 Mg x 2 vials Rocephin 1 gram x 2 vials Rocephin 500mg x 2 vials Rocephin 250mg x 5 vials Vistaril 50mg x 1 vial Depo Provera 150mg x 3 vials Benadryl 50 mg. x 1 vial Depo Testosterone 200 mg. x 3½ vials Delestrogen x 2½ vials B12 x 2½ vials B Complex x 2 vials Compazine 5mg X 1 vial Bacteriostat Water x 1 vial Sodium Chloride 0.9% Nitrostat Hepatitis B Vaccine x 3 injectables Hepatitis A Vaccine x 2 injectables Yellowfever x 2 vials Meningococcal Vaccine x 2 vials Thyphoid x 3 injectables Poliovirus Vaccine x 1 vial Tetanus Tyoid x 1 vial Tetanus Dip. x 5 vials MMR x 2 injectables Rubella Vaccine x 1 vial
Injectables. Unless specifically excluded, and when an oral alternative drug is not available, injectable medication is a covered benefit, including those medications intended to be self administered. Medications must be deemed medically necessary and appropriate to the Member's needs or condition for covered services, prescribed by a participating provider and approved in advance of treatment by HMO. If the drug therapy treatment is approved for self-administration, Member is required to obtain covered medications at a U.S. Healthcare participating pharmacy designated to fill injectable prescriptions. Experimental or investigational drugs or medications or drugs or medications that have not been proven safe and effective for a specific disease or approved for a mode of treatment by the FDA and the NIH are not covered under this contract. The off-label use of injectable drugs or medications is not covered. Drugs related to the treatment of noncovered services are not covered. Drugs related to the treatment of infertility, contraception and performance enhancing steroids are not covered. Needles, syringes and other injectable aids are not covered.
Injectables. Drugs other than oral medications (as indicated in HCPCS book for codes J0001-J8999 and Q codes or any replacement codes or any NDC equivalent codes) for non-chemotherapy medications, excluding clotting factors (J7190-J7199) and Blood Products.
Injectables. Injectables obtained from Non-Preferred Providers are not covered.

Related to Injectables

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  • Product ACCEPTANCE Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User(s) shall have thirty (30) days from the date of delivery to accept hardware products and sixty (60) days from the date of delivery to accept all other Product. Where the Contractor is responsible for installation, acceptance shall be from completion of installation. Failure to provide notice of acceptance or rejection or a deficiency statement to the Contractor by the end of the period provided for under this clause constitutes acceptance by the Authorized User(s) as of the expiration of that period. The License Term shall be extended by the time periods allowed for trial use, testing and acceptance unless the Commissioner or Authorized User agrees to accept the Product at completion of trial use. Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User shall have the option to run testing on the Product prior to acceptance, such tests and data sets to be specified by User. Where using its own data or tests, Authorized User must have the tests or representative set of data available upon delivery. This demonstration will take the form of a documented installation test, capable of observation by the Authorized User, and shall be made part of the Contractor’s standard documentation. The test data shall remain accessible to the Authorized User after completion of the test. In the event that the documented installation test cannot be completed successfully within the specified acceptance period, and the Contractor or Product is responsible for the delay, Authorized User shall have the option to cancel the order in whole or in part, or to extend the testing period for an additional thirty (30) day increment. Authorized User shall notify Contractor of acceptance upon successful completion of the documented installation test. Such cancellation shall not give rise to any cause of action against the Authorized User for damages, loss of profits, expenses, or other remuneration of any kind. If the Authorized User elects to provide a deficiency statement specifying how the Product fails to meet the specifications within the testing period, Contractor shall have thirty (30) days to correct the deficiency, and the Authorized User shall have an additional sixty (60) days to evaluate the Product as provided herein. If the Product does not meet the specifications at the end of the extended testing period, Authorized User, upon prior written notice to Contractor, may then reject the Product and return all defective Product to Contractor, and Contractor shall refund any monies paid by the Authorized User to Contractor therefor. Costs and liabilities associated with a failure of the Product to perform in accordance with the functionality tests or product specifications during the acceptance period shall be borne fully by Contractor to the extent that said costs or liabilities shall not have been caused by negligent or willful acts or omissions of the Authorized User’s agents or employees. Said costs shall be limited to the amounts set forth in the Limitation of Liability Clause for any liability for costs incurred at the direction or recommendation of Contractor.

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  • Samples Physical examples of materials, equipment, or workmanship that are representative of some portion of the Work and that establish the standards by which such portion of the Work will be judged. The Contractor shall furnish for approval all samples required by the Contract Documents. The Work shall be in accordance with approved samples.

  • Labeling Upon request, Lessee will xxxx the Equipment indicating Lessor's interest with labels provided by Lessor. Lessee will keep all Equipment free from any other marking or labeling which might be interpreted as a claim of ownership.

  • Waste Borrower shall not commit or suffer any waste of the Property or make any change in the use of the Property which will in any way materially increase the risk of fire or other hazard arising out of the operation of the Property, or take any action that might invalidate or give cause for cancellation of any Policy, or do or permit to be done thereon anything that may in any way impair the value of the Property or the security of this Security Instrument. Borrower will not, without the prior written consent of Lender, permit any drilling or exploration for or extraction, removal, or production of any minerals from the surface or the subsurface of the Land, regardless of the depth thereof or the method of mining or extraction thereof.

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