(on drugs packaging)

  • 81logistics — /loh jis tiks, leuh /, n. (used with a sing. or pl. v.) 1. the branch of military science and operations dealing with the procurement, supply, and maintenance of equipment, with the movement, evacuation, and hospitalization of personnel, with the …

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  • 82Hydrocodone/paracetamol — Hydrocodone / Paracetamol Combination of Hydrocodone Opioid analgesic Paracetamol Anilide analgesic Clinical data AHFS …

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  • 83Portrait of an American Family — Studio album by Marilyn Manson Releas …

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  • 84Antichrist Superstar — Studio album by Marilyn Manson Released …

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  • 85Poppers — For other uses, see Popper (disambiguation). Variety of popper brands Poppers is a slang term for various alkyl nitrites inhaled for recreational purposes, particularly isopropyl nitrite (2 propyl nitrite) and isobutyl nitrite (2 methylpropyl… …

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  • 86Hypervitaminosis D — DiseaseDisorder infobox Name = Hypervitaminosis D Caption = Cholecalciferol (shown above) and ergocalciferol are the two major forms of Vitamin D. ICD10 = ICD10|E|67|3|e|65 ICD9 = ICD9|278.4 ICDO = OMIM = DiseasesDB = 13939 MedlinePlus =… …

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  • 87Policies of the Shinawatra administration — As Prime Minister of the Kingdom of Thailand, Thaksin Shinawatra initiated many distinctive policies affecting the economy, public health, education, energy, drugs, and international relations. His policies have made him very popular with the… …

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  • 88List of Statutory Rules of Northern Ireland, 1997 — This is an incomplete list of Statutory Rules of Northern Ireland in 1997.1 100* Buses (Section 10B Permits) (Amendment) Regulations (Northern Ireland) 1997 S.R. 1997 No. 1 * Temporary Speed Limit (Upper Ballinderry, Lisburn) Order (Northern… …

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  • 89Orally disintegrating tablet — clonazepam ODT blister pack and tablet An orally disintegrating tablet or orodispersible tablet (ODT) is a drug dosage form available for a limited amount of over the counter (OTC) and prescription medications. ODTs differ from traditional… …

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  • 90Drug Master File — or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority in the intended drug market. There is no regulatory requirement to file a DMF. However, the document… …

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