|
description of hydrocodone Seen With Fentanyl Narcotic Pain Patch & 8226; FDA Reviews Adult Antidepressant-Suicide Link Hydrocodone Bitartrate and Acetaminophen Tablets USP Patient Information from WebMD & 8226; Hydrocodone is sometimes used to treat back pain. Find additional health information on back pain including other treatment options at WebMD.com. DESCRIPTION Hydrocodone bitartrate and acetaminophen is supplied in tablet form for oral administration. Hydrocodone bitartrate is an opioid analgesic and antitussive and occurs as fine description of hydrocodone, white crystals or as a crystalline powder. It is affected by light. The chemical name is 4 description of hydrocodone, 5a-Epoxy-3-methoxy-17-methylmorphinan-6-one tartrate (1: description of hydrocodone.
description of hydrocodone 1) hydrate (2:5). It has the following structural formula: Acetaminophen description of hydrocodone, 4´-Hydroxyacetanilide description of hydrocodone, a non-opiate description of hydrocodone, non-salicylate analgesic and antipyretic. It has the following structural formula: Hydrocodone Bitartrate and Acetaminophen Tablets USP for oral administration are available in a variety of strengths as described in the following table. Hydrocodone Strength Bitartrate Acetaminophen 2.5 mg 500 mg 2.5 mg 500 mg 5 mg 500 mg 5 mg 500 mg 7.5 mg 325 mg 7.5 mg 325 mg 7.5 mg 500 mg 7.5 mg 500 mg 7.5 mg 650 mg 7.5 mg 650 mg 7.5 mg 750 mg 7.5 mg 750 mg 10 mg 325 mg 10 mg 325 mg 10 mg 500 mg 10 mg 500 mg 10 mg 650 mg 10 mg 650 mg 10 mg 660 mg 10 mg 660 mg 10 mg 750 mg 10 mg 750 mg In addition description of hydrocodone, each tablet contains the following inactive ingredients: anhydrous lactose description of hydrocodone, croscarmellose sodium description of hydrocodone, crospovidone description of hydrocodone, magnesium stearate description of hydrocodone, microcrystalline cellulose description of hydrocodone, povidone description of hydrocodone, starch and stearic acid; except the 7.5 mg 325 mg description of hydrocodone, 10 mg 325 mg and 10 mg 500 mg tablets do not contain anhydrous lactose. The 7.5 mg 325 mg tablets include FD&C Yellow 6 Aluminum Lake; the 7.5 mg 650 mg tablets include FD&C Red 40 Aluminum Lake; the 10 mg 325 mg and 10 mg 750 mg tablets include D&C Yellow 10 Aluminum Lake; the 10 mg 500 mg tablets include FD&C Blue 2 Aluminum Lake; and the 10 mg 650 mg tablets include FD&C Blue 1 Alumin.
description of hydrocodone 750 mg 10 mg 750 mg In addition description of hydrocodone, each tablet contains the following inactive ingredients: anhydrous lactose description of hydrocodone, croscarmellose sodium description of hydrocodone, crospovidone description of hydrocodone, magnesium stearate description of hydrocodone, microcrystalline cellulose description of hydrocodone, povidone description of hydrocodone, starch and stearic acid; except the 7.5 mg 325 mg description of hydrocodone, 10 mg 325 mg and 10 mg 500 mg tablets do not contain anhydrous lactose. The 7.5 mg 325 mg tablets include FD&C Yellow 6 Aluminum Lake; the 7.5 mg 650 mg tablets include FD&C Red 40 Aluminum Lake; the 10 mg 325 mg and 10 mg 750 mg tablets include D&C Yellow 10 Aluminum Lake; the 10 mg 500 mg tablets include FD&C Blue 2 Aluminum Lake; and the 10 mg 650 mg tablets include FD&C Blue 1 Aluminu.
description of hydrocodone 
description of hydrocodone | | | | | |
description of hydrocodone
|