NDC 0121-4811 Hydrocodone Bitartrate And Homatropine Methylbromide

Hydrocodone Bitartrate And Homatropine Methylbromide

NDC Product Code 0121-4811

NDC CODE: 0121-4811

Proprietary Name: Hydrocodone Bitartrate And Homatropine Methylbromide What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Hydrocodone Bitartrate And Homatropine Methylbromide What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Hydrocodone is used to help relieve severe ongoing pain. Hydrocodone belongs to a class of drugs known as opioid (narcotic) analgesics. It works in the brain to change how your body feels and responds to pain. Do not use the extended-release form of hydrocodone to relieve pain that is mild or that will go away in a few days. This medication is not for occasional (as needed) use.

NDC Code Structure

  • 0121 - Pharmaceutical Associates, Inc.
    • 0121-4811 - Hydrocodone Bitartrate And Homatropine Methylbromide

NDC 0121-4811-40

Package Description: 4 TRAY in 1 CASE > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (0121-4811-05)

NDC Product Information

Hydrocodone Bitartrate And Homatropine Methylbromide with NDC 0121-4811 is a a human prescription drug product labeled by Pharmaceutical Associates, Inc.. The generic name of Hydrocodone Bitartrate And Homatropine Methylbromide is hydrocodone bitartrate and homatropine methylbromide. The product's dosage form is solution and is administered via oral form.

Labeler Name: Pharmaceutical Associates, Inc.

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

Product Type: Human Prescription Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

DEA Schedule: Schedule II (CII) Substances What is the Drug Enforcement Administration (DEA) CII Schedule?
The controlled substances in the CII schedule have a high abuse potential with severe psychological or physical dependence liability, but have accepted medical use in the United States. Schedule CII controlled substances include certain narcotic, stimulant, and depressant drugs.

Hydrocodone Bitartrate And Homatropine Methylbromide Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • HYDROCODONE BITARTRATE 5 mg/5mL
  • HOMATROPINE METHYLBROMIDE 1.5 mg/5mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)
  • CARAMEL (UNII: T9D99G2B1R)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SUCROSE (UNII: C151H8M554)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • SORBITOL (UNII: 506T60A25R)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Opioid Agonist - [EPC] (Established Pharmacologic Class)
  • Opioid Agonists - [MoA] (Mechanism of Action)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Pharmaceutical Associates, Inc.
Labeler Code: 0121
FDA Application Number: ANDA088008 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: ANDA - A product marketed under an approved Abbreviated New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 12-28-2009 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Information for Patients

Hydrocodone Combination Products

Hydrocodone Combination Products is pronounced as (hye droe koe' done)

Why is hydrocodone combination products medication prescribed?
Hydrocodone is available in combination with other ingredients, and different combination products are prescribed for different uses. Some hydrocodone combination product...
[Read More]

* Please review the disclaimer below.

Hydrocodone Bitartrate And Homatropine Methylbromide Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Other

Rx only

Rx OnlyOral prescription where permitted by state law.MANUFACTURED BYMorton Grove Pharmaceuticals, Inc.


Morton Grove, IL 60053


PACKAGED BYPharmaceutical


Associates, Inc.


Greenville, SC 29605


www.paipharma.com


R10/17

Warning Risks From Concomitant Use With Benzodiazepines Or Ot Her Cns Depressants

Concomitant use of opioids with benzodiazepines or other central nervous system (CNS) depressants, including alcohol, may result in profound sedation, respiratory depression, coma, and death (see


Warnings,


Precautions - Drug Interactions). Avoid use of opioid cough medications in patients taking benzodiazepines, other CNS depressants, or alcohol.

Description

This product contains hydrocodone (dihydrocodeinone) bitartrate, a semisynthetic centrally acting opioid antitussive. Homatropine Methylbromide is included in a subtherapeutic amount to discourage deliberate overdosage.Each 5 mL (teaspoonful) contains:


Hydrocodone Bitartrate, USP5 mgHomatropine Methylbromide, USP1.5 mgAlcoholless than 0.1%(contributed by flavorings)Also contains: Caramel, NF; Cherry Flavor; D&C Red No. 33; Glycerin, USP; Liquid Sugar; Methylparaben, NF; Propylene Glycol, USP; Propylparaben, NF and Sorbitol Solution, USP. Citric Acid, USP or Sodium Citrate, USP may be added for pH adjustment.


The hydrocodone component is 4,5α-epoxy-3-methoxy-17-methylmorphinan-6-one tartrate (1:1) hydrate (2:5), a fine white crystal or crystalline powder, which is derived from the opium alkaloid, thebaine, and has the following structural formula:C


18H


21NO


3 ∙ C


4H


6O


6 ∙ 2½ H


2O


M.W.494.50HYDROCODONE BITARTRATEHomatropine Methylbromide is 8-Azoniabicyclo[3.2.1]octane,3-[(hydroxyphenylacetyl)-oxy]-8,8-dimethyl-, bromide,endo-; a white crystal or fine white crystalline powder, and has the following structural formula:C


17H


24BrNO


3M.W. 370.29HOMATROPINE METHYLBROMIDE

Clinical Pharmacology

Hydrocodone is a semisynthetic opioid anti-tussive and analgesic with multiple actions qualitatively similar to those of codeine. The precise mechanism of action of hydrocodone and other opiates is not known; however, hydrocodone is believed to act directly on the cough center. In excessive doses, hydrocodone, like other opium derivatives, will depress respiration. The effects of hydrocodone in therapeutic doses on the cardiovascular system are insignificant. Hydrocodone can produce miosis, euphoria, physical and physiological dependence.Following a 10 mg oral dose of hydrocodone administered to five adult male subjects, the mean peak concentration was 23.6 ± 5.2 ng/mL. Maximum serum levels were achieved at 1.3 ± 0.3 hours and the half-life was determined to be 3.8 ± 0.3 hours. Hydrocodone exhibits a complex pattern of metabolism including O-demethylation, N-demethylation and 6-keto reduction to the corresponding 6-α-and 6-β-hydroxymetabolites.

Indications And Usage

Hydrocodone bitartrate and homatropine methylbromide syrup is indicated for the symptomatic relief of cough in adults and children 6 years of age and older.

Contraindications

Hydrocodone bitartrate and homatropine methylbromide syrup should not be administered to patients who are hypersensitive to hydrocodone or homatropine methylbromide.

Risks From Concomitant Use With Benzodiazepines Or Other Cns Depressants

Concomitant use of opioids, including hydrocodone bitartrate and homatropine methylbromide, with benzodiazepines, or other CNS depressants, including alcohol, may result in profound sedation, respiratory depression, coma, and death. Because of these risks, avoid use of opioid cough medications in patients taking benzodiazepines, other CNS depressants, or alcohol (see


Precautions - Drug Interactions).


Observational studies have demonstrated that concomitant use of opioid analgesics and benzodiazepines increases the risk of drug-related mortality compared to use of opioids alone. Because of similar pharmacologic properties, it is reasonable to expect similar risk with concomitant use of opioid cough medications and benzodiazepines, other CNS depressants, or alcohol.Advise both patients and caregivers about the risks of respiratory depression and sedation if hydrocodone bitartrate and homatropine methylbromide is used with benzodiazepines, alcohol, or other CNS depressants (see


Precautions - Information for Patients).


Hydrocodone can produce drug dependence of the morphine type and, therefore, has the potential for being abused. Psychic dependence, physical dependence and tolerance may develop upon repeated administration and it should be prescribed and administered with the same degree of caution appropriate to the use of other opioid drugs (see


DRUG ABUSE AND DEPENDENCE).

Respiratory Depression

The use of hydrocodone bitartrate and homatropine syrup is not recommended for use in children less than 6 years of age because of the risk of fatal respiratory depression (see


ADVERSE REACTIONS- Respiratory Depression). Hydrocodone bitartrate and homatropine methylbromide syrup produces dose-related respiratory depression by directly acting on brain stem respiratory centers. If respiratory depression occurs, it may be antagonized by the use of naloxone hydrochloride and other supportive measures when indicated.

Hydrocodone bitartrate and homatropine methylbromide syrup may produce dose-related respiratory depression by acting directly on brain stem respiratory centers (see


OVERDOSAGE). Use of Hydrocodone bitartrate and homatropine methylbromide syrup in children less than 6 years of age has been associated with fatal respiratory depression. Overdose with Hydrocodone bitartrate and homatropine methylbromide syrup in children 6 years of age and older, in adolescents, and in adults has been associated with fatal respiratory depression.


Postmarketing events seen in children under 6 years of age include accidental overdose, bronchopneumonia, coma, cyanosis, death, death neonatal, dyspnea, pulmonary edema, respiratory arrest, and respiratory depression. Postmarketing events seen in patients older than 6 years of age include accidental overdose, cardio-respiratory arrest, death due to drug toxicity, non-accidental overdose, and overdose.

Head Injury And Increased Intracranial Pressure

The respiratory depression properties of opioids and their capacity to elevate cerebrospinal fluid pressure may be markedly exaggerated in the presence of head injury, other intracranial lesions or a pre-existing increase in intracranial pressure. Furthermore, opioids produce adverse reactions which may obscure the clinical course of patients with head injuries.

Acute Abdominal Conditions

The administration of hydrocodone bitartrate and homatropine methylbromide syrup or other opioids may obscure the diagnosis or clinical course of patients with acute abdominal conditions.

Pediatric Use

In pediatric patients, as well as adults, the respiratory center is sensitive to the depressant action of opioid cough suppressants in a dose-dependent manner. Caution should be exercised when administering hydrocodone bitartrate and homatropine methylbromide syrup to pediatric patients 6 years of age and older because of the potential for fatal respiratory depression. Overdose of concomitant administration of hydrocodone bitartrate and homatropine methylbromide syrup with other respiratory depressants may increase the risk of respiratory depression in pediatric patients. Benefit to risk ratio should be carefully considered especially in pediatric population with respiratory embarrassment (e.g., croup) (see


PRECAUTIONS).

Safety and effectiveness of hydrocodone bitartrate and homatropine methylbromide in pediatric patients under six years of age have not been established. The use of hydrocodone bitartrate and homatropine methylbromide syrup in children less than 6 years of age has been associated with cases of fatal respiratory depression (see


ADVERSE REACTIONS - Respiratory Depression). Hydrocodone bitartrate and homatropine methylbromide syrup should be used with caution in pediatric patients 6 years of age and older (see


WARNINGS - Pediatric Use).

General

Before prescribing medication to suppress or modify cough, it is important to ascertain that the underlying cause of cough is identified, that modification of cough does not increase the risk of clinical or physiological complications, and that appropriate therapy for the primary disease is provided.

Special Risk Patients

Hydrocodone bitartrate and homatropine methylbromide syrup should be given with caution to certain patients such as the elderly or debilitated, and those with severe impairment of hepatic or renal functions, hypothyroidism, Addison's disease, prostatic hypertrophy or urethral stricture, asthma, and narrow-angle glaucoma.

Information For Patients

Inform patients and caregivers that potentially fatal additive effects may occur if hydrocodone bitartrate and homatropine methylbromide is used with benzodiazepines or other CNS depressants, including alcohol. Because of this risk, patients should avoid concomitant use of hydrocodone bitartrate and homatropine methylbromide with benzodiazepines or other CNS depressants, including alcohol (see


Warnings,


Precautions - Drug Interactions).


Hydrocodone may produce marked drowsiness and impair the mental and/or physical abilities required for the performance of potentially hazardous tasks such as driving a car or operating machinery. The patient using hydrocodone bitartrate and homatropine methylbromide syrup should be cautioned accordingly.Patients should be advised to measure hydrocodone bitartrate and homatropine methylbromide syrup with an accurate measuring device. A household teaspoon is not an accurate measuring device and could lead to overdosage, especially when a half a teaspoon is measured. A pharmacist can recommend an appropriate measuring device and can provide instructions for measuring the correct dose. Keep out of the reach of children.

Drug Interactions

The use of benzodiazepines, opioids, antihistamines, antipsychotics, anti-anxiety agents, or other CNS depressants (including alcohol) concomitantly with hydrocodone bitartrate and homatropine methylbromide may cause an additive CNS depressant effect, profound sedation, respiratory depression, coma, and death and should be avoided (see


Warnings).


The use of MAO inhibitors or tricyclic antidepressants with hydrocodone preparations may increase the effect of either the antidepressant or hydrocodone.

Carcinogenesis, Mutagenesis, Impairment Of Fertility

Studies of hydrocodone bitartrate and homatropine methylbromide in animals to evaluate the carcinogenic and mutagenic potential and the effect on fertility have not been conducted.

Pregnancy Category C

Animal reproduction studies have not been conducted with hydrocodone bitartrate and homatropine methylbromide. It is also not known whether hydrocodone bitartrate and homatropine methylbromide can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Hydrocodone bitartrate and homatropine methylbromide should be given to a pregnant woman only if clearly needed.

Nonteratogenic Effects

Babies born to mothers who have been taking opioids regularly prior to delivery, will be physically dependent. The withdrawal signs include irritability and excessive crying, tremors, hyperactive reflexes, increased respiratory rate, increased stools, sneezing, yawning, vomiting and fever. The intensity of the syndrome does not always correlate with the duration of maternal opioid use or dose.

Labor And Delivery

As with all opioids, administration of hydrocodone bitartrate and homatropine methylbromide to the mother shortly before delivery may result in some degree of respiratory depression in the newborn, especially if higher doses are used.

Nursing Mothers

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from hydrocodone bitartrate and homatropine methylbromide, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

Adverse Reactions

To report SUSPECTED ADVERSE REACTIONS, contact Pharmaceutical Associates, Inc. at 1-800-845-8210 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Central Nervous System

Sedation, drowsiness, mental clouding, lethargy, impairment of mental and physical performance, anxiety, fear, dysphoria, dizziness, psychic dependence, mood changes.

Gastrointestinal System

Nausea and vomiting may occur; they are more frequent in ambulatory than in recumbent patients. Prolonged administration of hydrocodone bitartrate and homatropine methylbromide may produce constipation.

Genitourinary System

Ureteral spasm, spasm of vesicle sphincters and urinary retention have been reported with opiates.

Dermatological

Skin rash, pruritus.

Drug Abuse And Dependence

Hydrocodone bitartrate and homatropine methylbromide syrup is a Schedule II opioid. Psychic dependence, physical dependence and tolerance may develop upon repeated administration of opioids; therefore, hydrocodone bitartrate and homatropine methylbromide syrup should be prescribed and administered with caution. However, psychic dependence is unlikely to develop when hydrocodone bitartrate and homatropine methylbromide is used for a short time for the treatment of cough. Physical dependence, the condition in which continued administration of the drug is required to prevent the appearance of a withdrawal syndrome, assumes clinically significant proportions only after several weeks of continued oral opioid use, although some mild degree of physical dependence may develop after a few days of opioid therapy.

Signs And Symptoms

Serious overdosage with hydrocodone is characterized by respiratory depression (a decrease in respiratory rate and/or tidal volume, Cheyne-Stokes respiration, cyanosis), extreme somnolence progressing to stupor or coma, skeletal muscle flaccidity, cold and clammy skin, and sometimes bradycardia and hypotension. In severe overdosage, apnea, circulatory collapse, cardiac arrest and death may occur. The ingestion of very large amounts of hydrocodone bitartrate and homatropine methylbromide syrup may, in addition, result in acute homatropine intoxication.

Treatment

Primary attention should be given to the reestablishment of adequate respiratory exchange through provision of a patent airway and the institution of assisted or controlled ventilation. The opioid antagonist naloxone hydrochloride is a specific antidote for respiratory depression which may result from overdosage or unusual sensitivity to opioids including hydrocodone. Therefore, an appropriate dose of naloxone hydrochloride should be administered, preferably by the intravenous route, simultaneously with efforts at respiratory resuscitation. For further information, see full prescribing information for naloxone hydrochloride. An antagonist should not be administered in the absence of clinically significant respiratory depression. Oxygen, intravenous fluids, vasopressors and other supportive measures should be employed as indicated. Gastric emptying may be useful in removing unabsorbed drug.

Dosage And Administration

It is important that Hydrocodone Bitartrate and Homatropine Methylbromide Oral Solution is measured with an accurate measuring device (see


PRECAUTIONS – Information for Patients). A household teaspoon is not an accurate measuring device and could lead to overdosage, especially when a half a teaspoon is measured. It is strongly recommended that an accurate measuring device be used. A pharmacist can provide an appropriate measuring device and can provide instructions for measuring the correct dose.


Adults and adolescents 12 years of age and over: 5 mL (1 teaspoonful) of the syrup every 4 to 6 hours as needed; do not exceed 30 mL (6 teaspoonfuls) in 24 hours.Children 6 to 11 years of age: 2.5 mL (½ teaspoonful) of the syrup every 4 to 6 hours as needed; do not exceed 15 mL (3 teaspoonfuls) in 24 hours.

How Supplied

Hydrocodone bitartrate and homatropine methylbromide syrup is a red-colored, cherry-flavored syrup supplied in the following oral dosage form:0121-4811-05:5 mL unit dose cup0121-4811-40:Case contains 40 unit dose cups of 5 mL (0121-4811-05) packaged in 4 trays of 10 unit dose cups each.

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. AVOID FREEZINGKEEP TIGHTLY CLOSEDDispense in a tight, light-resistant container as defined in the USP.

Medication Guide

  • HYDROCODONE AND HOMATROPINE(hye" droe koe' done hoe mat' roe peen)(hydrocodone bitartrate and homatropine methylbromide) syrup, CIIWhat is the most important information I should know about HYDROCODONE AND HOMATROPINE?
  • Taking HYDROCODONE AND HOMATROPINE with benzodiazepines or other central nervous system depressants, including alcohol can cause severe drowsiness, breathing problems (respiratory depression), coma, and death.HYDROCODONE AND HOMATROPINE can cause you to be drowsy. Avoid driving a car or operating machinery during the treatment with HYDROCODONE AND HOMATROPINE. Women who breastfeed should talk to their healthcare provider before taking HYDROCODONE AND HOMATROPINE.Call your healthcare provider or get emergency medical help right away if anyone taking HYDROCODONE AND HOMATROPINE has any of the symptoms below:
  • Increased sleepiness confusiondifficulty breathingshallow breathinglimpnessyour baby has difficulty breastfeedingKeep HYDROCODONE AND HOMATROPINE in a safe place away from children. Accidental use by a child is a medical emergency and can cause death. If a child accidentally takes HYDROCODONE AND HOMATROPINE, get emergency medical help right away.HYDROCODONE AND HOMATROPINE can cause serious side effects including death.Take HYDROCODONE AND HOMATROPINE exactly as prescribed by your healthcare provider. If you take the wrong dose of HYDROCODONE AND HOMATROPINE, you could overdose and die.HYDROCODONE AND HOMATROPINE is not for children under 6 years of age.What is HYDROCODONE AND HOMATROPINE?HYDROCODONE AND HOMATROPINE is a prescription medicine used to treat a cough in adults and children 6 years and older. HYDROCODONE AND HOMATROPINE contains hydrocodone and is a narcotic cough suppressant.HYDROCODONE AND HOMATROPINE is a federal controlled substance (C-II) because it contains hydrocodone that can be abused or lead to dependence. Keep HYDROCODONE AND HOMATROPINE in a safe place to prevent misuse and abuse. Selling or giving away HYDROCODONE AND HOMATROPINE may harm others, and is against the law. Tell your healthcare provider if you have ever abused or been dependent on alcohol, prescription medicines or street drugs.
  • HYDROCODONE AND HOMATROPINE is not for children under 6 years of age.Who should not take HYDROCODONE AND HOMATROPINE?Do not take HYDROCODONE AND HOMATROPINE if you are allergic to hydrocodone or homatropine methylbromide. See the end of this Medication Guide for a complete list of ingredients.Before you take HYDROCODONE AND HOMATROPINE, tell your healthcare provider about all of your medical conditions, including if you:have a drug dependencehave lung or breathing problems have had a head injuryhave pain in your stomach-area (abdomen) have a history of severe or persistent cough have prostate problemsplan to have surgery drink alcoholhave kidney or liver problems have diabeteshave thyroid problems, such as hypothyroidismhave problems with your urinary tract (urethral stricture)are pregnant or plan to become pregnant. It is not known if HYDROCODONE AND HOMATROPINE will harm your unborn baby. You and your healthcare provider should decide if you should take HYDROCODONE AND HOMATROPINE while you are pregnant. are breastfeeding or plan to breastfeed. It is not known if HYDROCODONE AND HOMATROPINE passes into your breast milk. You and your healthcare provider should decide if you will take HYDROCODONE AND HOMATROPINE or breastfeed. You should not do both.Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
  • Taking HYDROCODONE AND HOMATROPINE with certain other medicines can cause side effects or affect how well HYDROCODONE AND HOMATROPINE or the other medicines work.Do not start or stop other medicines without talking to your healthcare provider. Especially tell your healthcare provider if you:take pain medicines such as narcoticstake cold or allergy medicines that contain antihistamines or cough suppressants take medicines for mental illness (anti-psychotics, anti-anxiety)drink alcoholtake medicines for depression, including monoamine oxidase inhibitors (MAOIs) and tricyclicsAsk your healthcare provider if you are not sure if you take one of these medicines.How should I take HYDROCODONE AND HOMATROPINE?Take HYDROCODONE AND HOMATROPINE exactly as your healthcare provider tells you to take it.Your healthcare provider will tell you how much HYDROCODONE AND HOMATROPINE to take and when to take it. Do not change your dose without talking to your healthcare provider. Ask your pharmacist to give you a measuring device to help you measure the correct amount of HYDROCODONE AND HOMATROPINE.
  • Do not use a household teaspoon to measure your medicine. You may accidently take too much. If you take too much HYDROCODONE AND HOMATROPINE, call your healthcare provider or go to the nearest hospital emergency room right away.
  • What should I avoid while taking HYDROCODONE AND HOMATROPINE?HYDROCODONE AND HOMATROPINE can cause you to be drowsy. Avoid driving a car or operating machinery while you take HYDROCODONE AND HOMATROPINE until you know how it affects you.Avoid drinking alcohol while taking HYDROCODONE AND HOMATROPINE. Drinking alcohol can increase your chances of having serious side effects.What are the possible side effects of HYDROCODONE AND HOMATROPINE? HYDROCODONE AND HOMATROPINE may cause serious side effects, including:See "
  • What is the most important information I should know about HYDROCODONE AND HOMATROPINE?"
  • Breathing problems (respiratory depression) which can lead to death. Call your healthcare provider or get emergency treatment right away if you are sleeping more than usual, have shallow slow breathing, or confusion.
  • Physical dependence or abuse. Take HYDROCODONE AND HOMATROPINE exactly as your healthcare provider tells you to take it. Stopping HYDROCODONE AND HOMATROPINE suddenly could cause withdrawal symptoms.
  • Bowel problems including constipation or stomach pain. Increased intracranial pressure.The most common side effects of HYDROCODONE AND HOMATROPINE include:sleepinessconfusionnausea and vomitingdifficulty urinatingtrouble breathingThese are not all the possible side effects of HYDROCODONE AND HOMATROPINE.Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.How should I store HYDROCODONE AND HOMATROPINE?Store HYDROCODONE AND HOMATROPINE syrup at room temperature between 68°F to 77°F (20°C to 25°C).Keep HYDROCODONE AND HOMATROPINE syrup, and all medicines out of the reach of children.General information about the safe and effective use of HYDROCODONE AND HOMATROPINE. Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use HYDROCODONE AND HOMATROPINE for a condition for which it was not prescribed. Do not give HYDROCODONE AND HOMATROPINE to other people, even if they have the same symptoms that you have. It may harm them.
  • You can ask your pharmacist or healthcare provider for information about HYDROCODONE AND HOMATROPINE that is written for health professionals.What are the ingredients in HYDROCODONE AND HOMATROPINE? Active ingredient: hydrocodone bitartrate and homatropine methylbromide.
  • Inactive ingredients in HYDROCODONE AND HOMATROPINE syrup: Caramel, NF; Cherry Flavor; D&C Red No. 33; Glycerin, USP; Liquid Sugar; Methylparaben, NF; Propylene Glycol, USP; Propylparaben, NF and Sorbitol Solution, USP. Citric Acid, USP or Sodium Citrate, USP may be added for pH adjustment
  • MANUFACTURED BYMorton Grove Pharmaceuticals, Inc.
  • Morton Grove, IL 60053
  • PACKAGED BY Pharmaceutical
  • Associates, Inc.
  • Greenville, SC 29605
  • Www.paipharma.com
  • R10/17For more information, go to www.paipharma.com or call Pharmaceutical Associates, Inc. at 1-800-845-8210.This Medication Guide has been approved by the U.S. Food and Drug Administration

* Please review the disclaimer below.