Vicodin es how many mg

No special authorizations from Abbott are required. If you have any further questions regarding returns of this product, you may call Abbott Customer Service at Patient Communication Indication Important Safety Information Psychological dependence, physical dependence, and tolerance may develop upon repeated administration of narcotics; therefore, these products should be prescribed and administered with caution. Respiratory Depression: At high doses or in sensitive patients, hydrocodone may produce dose-related respiratory depression.

Head Injury and Increased Intracranial Pressure: The respiratory depressant effects of narcotics and their capacity to elevate cerebrospinal fluid pressure may be markedly exaggerated in the presence of head injury or other intracranial pressure.

Acute Abdominal Conditions: The administration of narcotics may obscure the diagnosis or clinical course of patients with acute abdominal conditions. As with any narcotic, special caution should be used when prescribing hydrocodone to elderly or debilitated patients and those with severe impairment of hepatic or renal function, hypothyroidism, Addison's disease, prostatic hypertrophy, or urethral stricture.

Caution should also be exercised with patients who are likely to take other acetaminophen-containing medications, antihistamines, antipsychotics, antianxiety agents, other narcotic analgesics, or other central nervous system CNS depressants including alcohol concomitantly.

When combined therapy is contemplated, the dose of one or both agents should be reduced. The use of monoamine oxidase MAO inhibitors or tricyclic antidepressants with hydrocodone preparations may increase the effect of either the antidepressant or hydrocodone. Babies born to mothers who have been taking opioids regularly prior to delivery will be physically dependent. Administration to the mother during labor or shortly before delivery may result in some degree of respiratory depression in the newborn.

The most frequently reported adverse reactions include lightheadedness, dizziness, sedation, nausea, and vomiting. On January 13, , the U. Food and Drug Administration FDA asked drug manufacturers to limit the strength of acetaminophen in prescription drug products, including combination acetaminophen and opioid products, to no more than mg per tablet, capsule, or other dosage unit. The FDA has stated that limiting the amount of acetaminophen per dosage unit in prescription products may reduce the risk of severe liver injury from acetaminophen overdosing.

What is the indication of the reformulated Vicodin? The indication for the new Vicodin formulations has remained the same: Vicodin, Vicodin ES , and Vicodin HP hydrocodone bitartrate and acetaminophen tablets, USP are indicated for the relief of moderate to moderately severe pain. It may cause dose-related respiratory depression in sensitive patients and caution should be exercised when prescribing to elderly or debilitated patients.

The concomitant use with other central nervous system CNS depressants and monoamine oxidase MAO inhibitors or tricyclic antidepressants may increase the effect of either drug.

Babies born to mothers who have been taking opioids regularly prior to delivery will be physically dependent. Dear Healthcare Provider:. What are the details about the new Vicodin? Formulations: The new Vicodin formulations contain mg of acetaminophen per tablet, which is lower than the amount mandated by the FDA. Tablet Visual Appearance and Markings: New Vicodin tablets will look slightly different than the original formulations.

Both are white, capsule-shaped, scored tablets. The original 7. How Supplied? The reformulated Vicodin is available in bottles of and tablets for each strength. The new National Drug Code NDC associated with each strength is listed in the chart below: Abbott is working with pharmacies to help ensure the availability of the new Vicodin formulations. What happened to the original Vicodin formulation? Abbott has been working with pharmacy wholesalers and pharmacies to process returns of the original Vicodin formulations, in order to minimize confusion or the potential for medication errors.

How do I return the original formulation of Vicodin? When returning the Vicodin formulations listed below, Abbott will issue credit to you through your wholesaler for full or partial bottles of product in original Abbott containers that have not expired. No special authorizations from Abbott are required.

Returns should be sent to:. Patient Communication. The new formulations of Vicodin will be available on October 8 th Patients should be instructed to call their physician if they have taken more than the recommended dose of acetaminophen.

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