The following Structured Product Label (SPL) was submitted to the FDA by Akorn for the product Acetylcysteine (NDC 17478-660). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding 1 indications and usage, 2.1 pre-treatment assessment and testing following acute acetaminophen ingestion, 2.2 nomogram for estimating potential for hepatotoxicity from acute acetaminophen ingestion and need for acetylcysteine treatment, other, 2.3 preparation and storage of acetylcysteine diluted solution prior to administration, 2.5 recommendations for repeated supratherapeutic acetaminophen ingestion, 3 dosage forms and strengths, 4 contraindications, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Acetylcysteine Injection is indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of acetaminophen in patients with acute ingestion or from repeated supratherapeutic ingestion (RSI).
The following recommendations are related to acute acetaminophen ingestion. For recommendations related to repeated supratherapeutic exposure see Dosage and Administration (2.5).
Acetylcysteine is an antidote for acetaminophen overdose. The critical ingestion-treatment interval for maximal protection against severe hepatic injury is between 0 to 8 hours. Efficacy diminishes progressively after 8 hours and treatment initiation between 15 and 24 hours post-ingestion of acetaminophen yields limited efficacy. However, it does not appear to worsen the condition of patients and it should not be withheld, since the reported time of ingestion may not be correct.
If the timing of the acute acetaminophen ingestion is known and the results of the acetaminophen assay are available within 8 hours:
The nomogram may underestimate the hepatotoxicity risk in patients with chronic alcoholism, malnutrition, or CYP2E1 enzyme inducing drugs (e.g., isoniazid), and consideration should be given to treating these patients even if the acetaminophen concentrations are in the nontoxic range.
Loading Dose
For patients whose acetaminophen concentrations are at or above the “possible” toxicity line (dotted line in nomogram):
For patients with an acute overdose from an extended-release acetaminophen, if the acetaminophen concentration at 4 hours post ingestion is below the possible toxicity line then obtain a second sample for acetaminophen concentration 8 to 10 hours after the acute ingestion. If the second value is at or above the “possible” toxicity line (dotted line in nomogram):
For patients whose values are below the “possible” toxicity line, but time of ingestion was unknown or sample was obtained less than 4 hours after ingestion:
For patients whose values are below the “possible” toxicity line and time of ingestion is known and the sample was obtained more than 4 hours after ingestion, do not administer acetylcysteine because there is minimal risk of hepatotoxicity.
Figure 1. Rumack-Matthew Nomogram for Estimating Potential for Hepatotoxicity for Acetaminophen Poisoning – Plasma or Serum Acetaminophen Concentration versus Time (hours) Post-acetaminophen Ingestion
(Adapted from Rumack and Matthew, Pediatrics 1975; 55: 871-876)
Maintenance Dose
Determine need for continued treatment with acetylcysteine after the loading dose. Choose ONE of the following based on the acetaminophen concentration:
The acetaminophen concentration is above the possible toxicity line according to the nomogram (see Figure 1):
The acetaminophen concentration could not be obtained:
For patients whose acetaminophen concentration is below the “possible” toxicity line (see Figure 1) and time of ingestion is known and the sample was obtained more than 4 hours after ingestion:
The acetaminophen concentration was in the non-toxic range, but time of ingestion was unknown or less than 4 hours:
Continued Therapy After Completion of Loading and Maintenance Doses
In cases of suspected massive overdose, or with concomitant ingestion of other substances, or in patients with preexisting liver disease; the absorption and/or the half-life of acetaminophen may be prolonged. In such cases, consideration should be given to the need for continued treatment with acetylcysteine beyond a total of three separate doses over a 21-hour infusion period.
Acetaminophen levels and ALT/AST and INR should be checked after the last maintenance dose. If acetaminophen levels are still detectable, or if the ALT/AST are still increasing or the INR remains elevated, dosing should be continued and the treating physician should contact a US regional poison center at 1-800-222-1222, alternatively, a special health professional assistance line for acetaminophen overdose at 1-800-525-6115 for assistance with dosing recommendations, or 1-800-932-5676 for additional information.
Acetylcysteine is for intravenous administration only.
Dosage Regimen
The total recommended dosage of acetylcysteine is 300 mg/kg given intravenously as 3 separate, sequential doses (i.e., 3-bag method to administer the loading, second, and third doses). The total recommended infusion time for 3 doses is 21 hours. For the recommended weight-based dosage and weight-based dilution in patients who weigh:
* Dilute acetylcysteine in one of the following three solutions: sterile water for injection, 0.45% sodium chloride injection, or 5% dextrose in water. | ||||||
** Recommended dosing for those less than 5 kg has not been studied. | ||||||
| Body Weight | Bag 1 (Loading Dose) | Bag 2 (Second Dose) | Bag 3 (Third Dose) | |||
| 150 mg/kg in 3 mL/kg of diluent* infused over 1 hour | 50 mg/kg in 7 mL/kg of diluent* infused over 4 hours | 100 mg/kg diluted in 14 mL/kg of diluent* infused over 16 hours | ||||
| Loading Dose | Diluent Volume | Second Dose | Diluent Volume | Third Dose | Diluent Volume | |
| 5 kg** | 750 mg | 15 mL | 250 mg | 35 mL | 500 mg | 70 mL |
| 10 kg | 1,500 mg | 30 mL | 500 mg | 70 mL | 1,000 mg | 140 mL |
| 15 kg | 2,250 mg | 45 mL | 750 mg | 105 mL | 1,500 mg | 210 mL |
| 20 kg | 3,000 mg | 60 mL | 1,000 mg | 140 mL | 2,000 mg | 280 mL |
* Dilute acetylcysteine in one of the following three solutions: sterile water for injection, 0.45% sodium chloride injection, or 5% dextrose in water. | |||
| Body Weight | Bag 1 (Loading Dose) | Bag 2 (Second Dose) | Bag 3 (Third Dose) |
| 150 mg/kg in 100 mL of diluent* infused over 1 hour | 50 mg/kg in 250 mL of diluent* infused over 4 hours | 100 mg/kg in 500 mL of diluent* infused over 16 hours | |
| 21 kg | 3,150 mg | 1,050 mg | 2,100 mg |
| 30 kg | 4,500 mg | 1,500 mg | 3,000 mg |
| 40 kg | 6,000 mg | 2,000 mg | 4,000 mg |
* Dilute acetylcysteine in one of the following three solutions: sterile water for injection, 0.45% sodium chloride injection, or 5% dextrose in water. | |||
** No specific studies have been conducted to evaluate the necessity of dose adjustments in patients weighing over 100 kg. Limited information is available regarding the dosing requirements of patients that weigh more than 100 kg. | |||
| Body Weight | Bag 1 (Loading Dose) | Bag 2 (Second Dose) | Bag 3 (Third Dose) |
| 150 mg/kg in 200 mL of diluent* infused over 1 hour | 50 mg/kg in 500 mL of diluent* infused over 4 hours | 100 mg/kg in 1,000 mL of diluent* infused over 16 hours | |
| 41 kg | 6,150 mg | 2,050 mg | 4,100 mg |
| 50 kg | 7,500 mg | 2,500 mg | 5,000 mg |
| 60 kg | 9,000 mg | 3,000 mg | 6,000 mg |
| 70 kg | 10,500 mg | 3,500 mg | 7,000 mg |
| 80 kg | 12,000 mg | 4,000 mg | 8,000 mg |
| 90 kg | 13,500 mg | 4,500 mg | 9,000 mg |
| ≥100 kg** | 15,000 mg | 5,000 mg | 10,000 mg |
Loading Dose/Infusion Rate Study
In a randomized, open-label, multi-center clinical study conducted in Australia in patients with acetaminophen poisoning, the rates of hypersensitivity reactions between a 15-minute and 60-minute intravenous infusion for the 150 mg/kg loading dose of acetylcysteine were compared.
The incidence of drug-related adverse reactions occurring within the first 2 hours following acetylcysteine administration is presented in Table 5. Overall, 17% of patients developed an acute hypersensitivity reaction (18% in the 15-minute infusion group; 14% in the 60-minute infusion group) [see Warnings and Precautions (5.1), Clinical Studies (14)].
Unkn=Unknown | |||||||||||
| Treatment Group | 15-mins | 60-mins | |||||||||
| Number of Patients | n=109 | n=71 | |||||||||
| Cardiac disorders | 5 (5%) | 2 (3%) | |||||||||
| Severity: | Unkn | Mild | Moderate | Severe | Unkn | Mild | Moderate | Severe | |||
| Tachycardia NOS | 4 (4%) | 1 (1%) | 2 (3%) | ||||||||
| Gastrointestinal disorders | 16 (15%) | 7 (10%) | |||||||||
| Severity: | Unkn | Mild | Moderate | Severe | Unkn | Mild | Moderate | Severe | |||
| Nausea | 1 (1%) | 6 (6%) | 1 (1%) | 1 (1%) | |||||||
| Vomiting NOS | 2 (2%) | 11 (10%) | 2 (3%) | 4 (6%) | |||||||
| Immune System Disorders | 20 (18%) | 10 (14%) | |||||||||
| Severity: | Unkn | Mild | Moderate | Severe | Unkn | Mild | Moderate | Severe | |||
| Hypersensitivity reaction | 2 (2%) | 6 (6%) | 11 (10%) | 1 (1%) | 4 (6%) | 5 (7%) | 1 (1%) | ||||
| Respiratory, thoracic and mediastinal disorders | 2 (2%) | 2 (3%) | |||||||||
| Severity: | Unkn | Mild | Moderate | Severe | Unkn | Mild | Moderate | Severe | |||
| Pharyngitis | 1 (1%) | ||||||||||
| Rhinorrhea | 1 (1%) | ||||||||||
| Rhonchi | 1 (1%) | ||||||||||
| Throat tightness | 1 (1%) | ||||||||||
| Skin & subcutaneous tissue disorders | 6 (6%) | 5 (7%) | |||||||||
| Severity: | Unkn | Mild | Moderate | Severe | Unkn | Mild | Moderate | Severe | |||
| Pruritus | 1 (1%) | 2 (3%) | |||||||||
| Rash NOS | 3 (3%) | 2 (2%) | 3 (4%) | ||||||||
| Vascular disorders | 2 (2%) | 3 (4%) | |||||||||
| Severity: | Unkn | Mild | Moderate | Severe | Unkn | Mild | Moderate | Severe | |||
| Flushing | 1 (1%) | 1 (1%) | 2 (3%) | 1 (1%) | |||||||
Safety Study
A large multi-center study was performed in Canada where data were collected from patients who were treated with intravenous acetylcysteine for acetaminophen overdose between 1980 and 2005. This study evaluated 4,709 adult cases and 1,905 pediatric cases. The incidence of hypersensitivity reactions in adult (overall incidence 8%) and pediatric (overall incidence 10%) patients is presented in Tables 6 and 7.
| Incidence (%) | |
| Reaction | % of Patients (N=4,709) |
| Urticaria/Facial Flushing | 6.1% |
| Pruritus | 4.3% |
| Respiratory Symptoms* | 1.9% |
| Edema | 1.6% |
| Hypotension | 0.1% |
| Anaphylaxis | 0.1% |
* Respiratory symptoms are defined as presence of any of the following: cough, wheezing, stridor, shortness of breath, chest tightness, respiratory distress, or bronchospasm. | |
| Incidence (%) | |
| Reaction | % of Patients (N=1,905) |
| Urticaria/Facial Flushing | 7.6% |
| Pruritus | 4.1% |
| Respiratory Symptoms* | 2.2% |
| Edema | 1.2% |
| Anaphylaxis | 0.2% |
| Hypotension | 0.1% |
Risk Summary
Limited published case reports and case series of pregnant women exposed to acetylcysteine during various trimesters are not sufficient to inform any drug associated risk. Delaying treatment of acetaminophen overdose may increase the risk of maternal or fetal morbidity and mortality [see Clinical Considerations]. Reproduction studies in rats and rabbits following oral administration of acetylcysteine during the period of organogenesis at doses similar to the total intravenous dose (based on the body surface area) did not cause any adverse effects to the fetus. The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.
Clinical Considerations
Disease-Associated Maternal and/or Embryo/Fetal Risk
Acetaminophen and acetylcysteine cross the placenta. Delaying treatment in pregnant women with acetaminophen overdose and potentially toxic acetaminophen plasma levels may increase the risk of maternal and fetal morbidity and mortality.
Data
Animal Data
Reproduction studies have been performed following administration of acetylcysteine during the period of organogenesis in rats at oral doses up to 2,000 mg/kg/day (1.1 times the recommended total human intravenous dose of 300 mg/kg based on body surface area comparison) and in rabbits at oral doses up to 1,000 mg/kg/day (1.1 times the recommended total human intravenous dose of 300 mg/kg based on body surface area comparison). No adverse developmental outcomes due to acetylcysteine were observed.
Risk Summary
There are no data on the presence of acetylcysteine in human milk, the effects on the breastfed infant, or the effects on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for acetylcysteine and any potential adverse effects on the breastfed child from acetylcysteine or from the underlying maternal condition.
Clinical Considerations
Based on the pharmacokinetic data, acetylcysteine should be nearly completely cleared 30 hours after administration. Breastfeeding women may consider pumping and discarding their milk for 30 hours after administration.
Distribution
The steady-state volume of distribution (Vdss) following administration of an intravenous dose of acetylcysteine was 0.47 liter/kg. The protein binding of acetylcysteine ranges from 66% to 87%.
Elimination
Metabolism
Acetylcysteine (i.e., N-acetylcysteine) is postulated to form cysteine and disulfides (N,N-diacetylcysteine and N-acetylcysteine). Cysteine is further metabolized to form glutathione and other metabolites.
Excretion
After a single oral dose of [35S]-acetylcysteine 100 mg, between 13% to 38% of the total radioactivity administered was recovered in urine within 24 hours. In a separate study, renal clearance was estimated to be approximately 30% of total body clearance.
Specific Populations:
Hepatic Impairment
Following a 600 mg intravenous dose of acetylcysteine to subjects with mild (Child Pugh Class A, n=1), moderate (Child-Pugh Class B, n=4) or severe (Child-Pugh Class C; n=4) hepatic impairment and 6 healthy matched controls, mean T1/2 increased by 80%. Also, the mean CL decreased by 30% and the systemic acetylcysteine exposure (mean AUC) increased 1.6-fold in subjects with hepatic impairment compared to subjects with normal hepatic function. These changes are not considered to be clinically meaningful.
Renal Impairment
Hemodialysis may remove some of total acetylcysteine.
Loading Dose/Infusion Rate Study
A randomized, open-label, multi-center clinical study was conducted in Australia in patients with acetaminophen poisoning to compare the rates of hypersensitivity reactions between two rates of infusion for the intravenous acetylcysteine loading dose. One hundred nine subjects were randomized to a 15-minute infusion rate and seventy-one subjects were randomized to a 60-minute infusion rate. The loading dose was 150 mg/kg followed by a maintenance dose of 50 mg/kg over 4 hours and then 100 mg/kg over 16 hours. Of the 180 patients, 27% were male and 73% were female. Ages ranged from 15 to 83 years, with the mean age being 30 years (±13.0).
A subgroup of 58 subjects (33 in the 15-minute infusion group; 25 in the 60-minute infusion group) was treated within 8 hours of acetaminophen ingestion. No hepatotoxicity occurred within this subgroup; however, with 95% confidence, the true hepatotoxicity rates could range from 0% to 9% for the 15-minute infusion group and from 0% to 12% for the 60-minute infusion group.
Observational Study
An open-label, observational database contained information on 1,749 patients who sought treatment for acetaminophen overdose over a 16-year period. Of the 1,749 patients, 65% were female, 34% were male and less than 1% was transgender. Ages ranged from 2 months to 96 years, with 72% of the patients falling in the 16- to 40-year-old age bracket. A total of 399 patients received acetylcysteine treatment. A post-hoc analysis identified 56 patients who (1) were at high or probable risk for hepatotoxicity (APAP greater than 150 mg/L at the four hours line according to the Australian nomogram) and (2) had a liver function test. Of the 53 patients who were treated with intravenous acetylcysteine (300 mg/ kg intravenous acetylcysteine administered over 20 to 21 hours) within 8 hours, two (4%) developed hepatotoxicity (AST or ALT greater than 1,000 U/L). Twenty-one of 48 (44%) patients treated with acetylcysteine after 15 hours developed hepatotoxicity. The actual number of hepatotoxicity outcomes may be higher than what is reported here. For patients with multiple admissions for acetaminophen overdose, only the first overdose treated with intravenous acetylcysteine was examined. Hepatotoxicity may have occurred in subsequent admissions.
Evaluable data were available from a total of 148 pediatric patients (less than 16 years of age) who were admitted for poisoning following ingestion of acetaminophen, of whom 23 were treated with intravenous acetylcysteine. There were no deaths of pediatric patients. None of the pediatric patients receiving intravenous acetylcysteine developed hepatotoxicity while two patients not receiving intravenous acetylcysteine developed hepatotoxicity. The number of pediatric patients is too small to provide a statistically significant finding of efficacy; however the results appear to be consistent to those observed for adults.
Hypersensitivity Reactions
Advise patients and caregivers that hypersensitivity reactions related to administration and infusion may occur during and after acetylcysteine treatment, including hypotension, wheezing, shortness of breath and bronchospasm [see Warnings and Precautions (5.1)].
For specific treatment information regarding the clinical management of acetaminophen overdose, please contact your regional poison center at 1-800-222-1222, or alternatively, a special health professional assistance line for acetaminophen overdose at 1-800-525-6115.
AKORN
Manufactured by: Akorn, Inc.
Lake Forest, IL 60045
AY00N Rev. 02/17
Because acetylcysteine is hyperosmolar (2,600 mOsmol/L), acetylcysteine must be diluted in sterile water for injection, 0.45% sodium chloride injection (1/2 normal saline), or 5% dextrose in water prior to intravenous administration [see Warnings and Precautions (5.2)]. Dilution in these three solutions results in different osmolarity of the solution for intravenous administration (see Table 1 for examples of different osmolarity of the solution depending on the type of solution and the acetylcysteine concentration).
Visually inspect for particulate matter and discoloration prior to administration. The color of the diluted solution ranges from colorless to a slight pink or purple once the stopper is punctured (the color change does not affect the quality of the product). The diluted solution can be stored for 24 hours at room temperature. Discard unused portion. If a vial was previously opened, do not use for intravenous administration.
* Adjust osmolarity to a physiologically safe level (generally not less than 150 mOsmol/L in pediatric patients). | |||
| Acetylcysteine Concentration | Osmolarity | ||
| Sterile Water for Injection | ½ Normal Saline | D5W | |
| 7 mg/mL | 91 mOsmol/L* | 245 mOsmol/L | 343 mOsmol/L |
| 24 mg/mL | 312 mOsmol/L | 466 mOsmol/L | 564 mOsmol/L |
Repeated supratherapeutic acetaminophen ingestion (RSI) is an ingestion of acetaminophen at dosages higher than those recommended for extended periods of time. The risk of hepatotoxicity and the recommendations for treatment of acute acetaminophen ingestion (i.e., the Rumack-Matthew nomogram) do not apply to patients with RSI. Therefore, obtain the following information to guide acetylcysteine treatment for RSI:
For specific acetylcysteine dosage and administration information in patients with RSI, consider contacting your regional poison center at 1-800-222-1222, or alternatively, a special health professional assistance line for acetaminophen overdose at 1-800-525-6115.
Injection: 200 mg/mL (6 grams of acetylcysteine in 30 mL) in a single-dose vial.
Acetylcysteine Injection is contraindicated in patients with a previous hypersensitivity reaction to acetylcysteine [see Warnings and Precautions (5.1)].
Serious acute hypersensitivity reactions during acetylcysteine administration including rash, hypotension, wheezing, and/or shortness of breath, have been observed in patients receiving intravenous acetylcysteine for acetaminophen overdose and occurred soon after initiation of the infusion [see Adverse Reactions (6.1)]. If a severe hypersensitivity reaction occurs, immediately stop the infusion of acetylcysteine and initiate appropriate treatment.
One patient with asthma developed bronchospasm and died after intravenous administration of acetylcysteine. Acetylcysteine should be used with caution in patients with asthma, or where there is a history of bronchospasm. Patients with asthma should be closely monitored during initiation of acetylcysteine therapy and throughout acetylcysteine therapy.
Acute flushing and erythema of the skin may occur in patients receiving acetylcysteine intravenously. These reactions usually occur 30 to 60 minutes after initiating the infusion and often resolve spontaneously despite continued infusion of acetylcysteine. If a reaction to acetylcysteine involves more than simply flushing and erythema of the skin, it should be treated as a hypersensitivity reaction.
Management of less severe hypersensitivity reactions should be based upon the severity of the reaction and include temporary interruption of the infusion and/or administration of antihistaminic drugs. The acetylcysteine infusion may be carefully restarted after treatment of the hypersensitivity symptoms has been initiated; however, if the hypersensitivity reaction returns upon re-initiation of treatment or increases in severity, acetylcysteine should be discontinued and alternative patient management should be considered.
The total volume of acetylcysteine administered should be adjusted for patients less than 40 kg and for those requiring fluid restriction. To avoid fluid overload, the volume of diluent should be reduced as needed [see Dosage and Administration (2)]. If volume is not adjusted fluid overload can occur, potentially resulting in hyponatremia, seizure and death.
Intravenous administration of acetylcysteine can cause fluid overload, potentially resulting in hyponatremia, seizure and death. To avoid fluid overload, use the recommended dilution shown in Tables 2, 3 and 4 [see Dosage and Administration (2.4)].
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
In the literature the most frequently reported adverse reactions attributed to intravenous acetylcysteine administration were rash, urticaria and pruritus. The frequency of adverse reactions has been reported to be between 0.2% and 21%, and they most commonly occur during the initial loading dose of acetylcysteine.
Safety and effectiveness of acetylcysteine in pediatric patients have not been established by adequate and well-controlled studies. Use of acetylcysteine in pediatric patients 5 kg and greater is based on clinical practice [see Dosage and Administration (2.4)].
Single intravenous doses of acetylcysteine at 1,000 mg/kg in mice, 2,445 mg/kg in rats, 1,500 mg/kg in guinea pigs, 1,200 mg/kg in rabbits and 500 mg/kg in dogs were lethal. Symptoms of acute toxicity in the animals were ataxia, hypoactivity, labored respiration, cyanosis, loss of righting reflex and convulsions.
Acetylcysteine injection is an intravenous antidote for the treatment of acetaminophen overdose. Acetylcysteine is the nonproprietary name for the N-acetyl derivative of the naturally occurring amino acid, L-cysteine (N-acetyl-L-cysteine). The compound is a white crystalline powder, which melts in the range of 104° to 110°C and has a very slight odor. The molecular formula of the compound is C5H9NO3S, and its molecular weight is 163.2. Acetylcysteine has the following structural formula:
Acetylcysteine Injection is supplied as a sterile solution in vials containing 20% w/v (200 mg/mL) acetylcysteine. The pH of the solution ranges from 6.0 to 7.5. Acetylcysteine Injection contains the following inactive ingredients: 0.5 mg/mL disodium edetate, sodium hydroxide (used for pH adjustment), and Sterile Water for Injection, USP.
Acetylcysteine has been shown to reduce the extent of liver injury following acetaminophen overdose. Acetaminophen doses of 150 mg/kg or greater have been associated with hepatotoxicity. Acetylcysteine probably protects the liver by maintaining or restoring the glutathione levels, or by acting as an alternate substrate for conjugation with, and thus detoxification of, the reactive metabolite of acetaminophen.
After a single intravenous dose of acetylcysteine, the plasma concentration of total acetylcysteine declined in a poly-exponential decay manner with a mean terminal half-life (T1/2) of 5.6 hours. The mean clearance (CL) for acetylcysteine was 0.11 liter/hr/kg and renal CL constituted about 30% of the total CL.
Long-term studies in animals have not been performed to evaluate the carcinogenic potential of acetylcysteine. Acetylcysteine was not genotoxic in the Ames test or the in vivo mouse micronucleus test. It was, however, positive in the in vitro mouse lymphoma cell (L5178Y/TK+/-) forward mutation test.
Treatment of male rats with acetylcysteine at an oral dose of 250 mg/kg/day for 15 weeks (0.1 times the recommended total human intravenous dose of 300 mg/kg based on body surface comparison) did not affect the fertility or general reproductive performance.
Acetylcysteine Injection is available as a 20% solution (200 mg/mL) in 30 mL single-dose glass vials. Each single-dose vial contains 6 g/30 mL (200 mg/mL) of acetylcysteine. Acetylcysteine Injection is sterile and can be used for intravenous administration. It is available as follows:
| NDC 17478-660-30 | 30 mL vials, carton of 4 |
Do not use previously opened vials for intravenous administration.
Note: The color of Acetylcysteine Injection may turn from essentially colorless to a slight pink or purple once the stopper is punctured. The color change does not affect the quality of the product.
The stopper in the Acetylcysteine Injection vial is formulated with a synthetic base-polymer and does not contain Natural Rubber Latex, Dry Natural Rubber, or blends of Natural Rubber.
Storage
Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Principal Display Panel Text for Container Label:
NDC 17478-660-30
Acetylcysteine
Injection
6 g/30 mL
(200 mg/mL)
Must be Further Diluted Prior to
Intravenous Use
30 mL Single dose Vial
Principal Display Panel Text for Carton Label:
NDC 17478-660-30
Acetylcysteine
Injection
6 g/30 mL
(200 mg/mL)
Must be Further Diluted Prior to
Intravenous Use
Preservative Free
4 x 30 mL Single dose Vial
Sterile
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