Vicodin

(redirected from hydrocodone bitartrate and acetaminophen)
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Related to hydrocodone bitartrate and acetaminophen: Vicodin

Vic·o·din

(vī′kə-dn)

A trademark for a drug containing hydrocodone bitartrate and acetaminophen.

American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

References in periodicals archive ?

Pharmaceutical products company Lannett Company Inc (NYSE:LCI) disclosed on Monday the receipt of approval from the US Food and Drug Administration (FDA) of its Abbreviated New Drug Application (ANDA) for Hydrocodone Bitartrate and Acetaminophen Tablets USP in 5 mg/325 mg, 7.5 mg/325 mg and 10 mg/325 mg.

Lannett wins US FDA approval for additional dosage strengths of Hydrocodone Bitartrate and Acetaminophen Tablets USP

M2 PHARMA-June 27, 2017-Lannett wins US FDA approval for additional dosage strengths of Hydrocodone Bitartrate and Acetaminophen Tablets USP

Lannett wins US FDA approval for additional dosage strengths of Hydrocodone Bitartrate and Acetaminophen Tablets USP

Vicodin, a combination of the powerful opioid pain reliever hydrocodone bitartrate and acetaminophen, is being reclassified as "possibly'' highly addictive and prone to abuse, and will now be considered a schedule II drug.

Addiction risk prompts reclassification of Vicodin

The FDA announced a voluntary, nationwide recall of certain lots of hydrocodone bitartrate and acetaminophen tablets and also certain lots of phenobarbital tablets.

Qualitest Pharma drugs recalled

Food & Drug Administration (FDA) for QSC-001, a unique orally disintegrating tablet (ODT) formulation of hydrocodone bitartrate and acetaminophen (HB/APAP) for the treatment of moderate to moderately severe pain.

QUESTCOR INITIATES QSC-001 CLINICAL PROGRAM

1 prescribed drug in the U.S.: hydrocodone bitartrate and acetaminophen tablets, USP.