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NDC 70199-0007-30 Robinul 1 mg/1 Details
Robinul 1 mg/1
Robinul is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Casper Pharma LLC. The primary component is GLYCOPYRROLATE.
MedlinePlus Drug Summary
Glycopyrrolate is used in combination with other medications to treat ulcers in adults and children 12 years of age and older. Glycopyrrolate (Cuvposa) is used to reduce saliva and drooling in children between 3 and16 years of age that have certain medical conditions that cause drooling. Glycopyrrolate is in a class of medications called anticholinergics. It decreases stomach acid and saliva production by blocking the activity of a certain natural substance in the body.
Related Packages: 70199-0007-30Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Glycopyrrolate
Product Information
| NDC | 70199-0007 |
|---|---|
| Product ID | 70199-007_1c57b7db-a3c3-4635-b324-a3ebfa585feb |
| Associated GPIs | 49102030000310 |
| GCN Sequence Number | 004887 |
| GCN Sequence Number Description | glycopyrrolate TABLET 1 MG ORAL |
| HIC3 | J2B |
| HIC3 Description | ANTICHOLINERGICS,QUATERNARY AMMONIUM |
| GCN | 19130 |
| HICL Sequence Number | 002028 |
| HICL Sequence Number Description | GLYCOPYRROLATE |
| Brand/Generic | Brand |
| Proprietary Name | Robinul |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Glycopyrrolate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | mg/1 |
| Substance Name | GLYCOPYRROLATE |
| Labeler Name | Casper Pharma LLC |
| Pharmaceutical Class | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA012827 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 70199-0007-30 (70199000730)
| NDC Package Code | 70199-007-30 |
|---|---|
| Billing NDC | 70199000730 |
| Package | 30 TABLET in 1 CONTAINER (70199-007-30) |
| Marketing Start Date | 2020-10-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 94fb029a-6371-4b1c-89de-35e8209c7cab Details
HIGHLIGHTS OF PRESCRIBING INFORMATION
ROBINUL® and ROBINUL® FORTE (glycopyrrolate) tablets, for oral use
Initial U.S. Approval: 1961
INDICATIONS AND USAGE
ROBINUL and ROBINUL FORTE are anticholinergics indicated in adults to reduce symptoms of a peptic ulcer as an adjunct to treatment of peptic ulcer. (1)
Limitations of Use:
Not indicated as monotherapy for the treatment of peptic ulcer because effectiveness in peptic ulcer healing has not been established. (1)
DOSAGE AND ADMINISTRATION
Important Dosing Information (2.1)
• ROBINUL FORTE is not recommended for patients initiating treatment or receiving maintenance treatment with ROBINUL or another 1 mg dosage strength of oral glycopyrrolate tablets.
Recommended Dosage (2.2)
• The recommended initial dosage of ROBINUL is 1 mg three times daily (in the morning, early afternoon, and at bedtime). Some patients may require 2 mg at bedtime to assure overnight control of symptoms. For maintenance, a dosage of 1 mg twice a day is frequently adequate.
• The recommended dosage of ROBINUL FORTE for adults is 2mg two or three times daily at equally spaced intervals.
• The maximum recommended daily dosage is 8 mg.
• Use the lowest effective dosage of glycopyrrolate to control symptoms. If patients can be titrated to a lower dose, switch from ROBINUL FORTE to ROBINUL or another 1 mg oral tablet of glycopyrrolate.
DOSAGE FORMS AND STRENGTHS
• Tablets: 1 mg (functionally scored) and 2 mg (3)
CONTRAINDICATIONS
WARNINGS AND PRECAUTIONS
• Precipitation of Acute Glaucoma: May increase intraocular pressure; if symptoms occur, discontinue use and promptly seek medical care. (4, 5.1)
• Partial or Complete Mechanical Intestinal Obstruction: Diarrhea may be an early symptom, especially in patients with ileostomy or colostomy. If the obstruction is suspected, discontinue use and evaluate the patient for obstruction. (4, 5.2)
• GI Adverse Reactions Due to Decreased GI Motility: Delayed gastric emptying, constipation, and intestinal pseudo-obstruction may occur and precipitate or aggravate paralytic ileus and toxic megacolon; not recommended for use with anticholinergics or other medications that decrease GI peristalsis. (4, 5.3, 7.1)
• Cognitive and Visual Adverse Reactions: May impair mental and/or physical function. Inform patients not to operate motor vehicles or perform other hazardous tasks until reasonably certain they are not adversely affected; discontinue use if signs or symptoms develop. (5.4, 7.1)
• Heat Prostration at High Environmental Temperatures: Heat prostration resulting in fever and heatstroke can occur, especially in geriatric patients. Avoid exposure to hot or very warm environmental temperatures. (5.5, 5.7)
• Other Conditions Exacerbated by Anticholinergic Adverse Reactions: Use is not recommended in patients with autonomic neuropathy, hyperthyroidism, cardiac disease, hiatal hernia, etc. (5.6, 7.1)
• Increased Risk of Anticholinergic Adverse Reactions in Geriatric Patients: Complications include urinary retention, bowel obstruction, heat prostration, arrhythmias, delirium, and falls or fractures. Not recommended in geriatric patients and may be contraindicated in some patients with underlying medical conditions. (4, 5.7, 8.5)
ADVERSE REACTIONS
Adverse reactions include blurred vision, drowsiness, decreased sweating, flushing, vomiting, constipation, dry mouth, tachycardia, and urinary retention. (6)
To report SUSPECTED ADVERSE REACTIONS, contact Casper Pharma LLC at 1-844-5-CASPER (1-844-522-7737) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
DRUG INTERACTIONS
USE IN SPECIFIC POPULATIONS
• Renal Impairment: Monitor patients with renal impairment; if anticholinergic adverse reactions occur, discontinue use. (8.6)
See 17 for PATIENT COUNSELING INFORMATION.
Revised: 10/2022
Table Of Contents
FULL PRESCRIBING INFORMATION: CONTENTS*
1 INDICATIONS & USAGE
2 DOSAGE & ADMINISTRATION
2.1 Important Dosing Information
2.2 Recommended Dosage
3 DOSAGE FORMS & STRENGTHS
4 CONTRAINDICATIONS
5 WARNINGS AND PRECAUTIONS
5.1 Precipitation of Acute Glaucoma
5.2 Partial or Complete Mechanical Intestinal Obstruction
5.3 Gastrointestinal Adverse Reactions Due to Decreased Gastrointestinal Motility
5.4 Cognitive and Visual Adverse Reactions
5.5 Heat Prostration at High Environmental Temperatures
5.6 Other Conditions Exacerbated by Anticholinergic Adverse Reactions
5.7 Increased Risk of Anticholinergic Adverse Reactions in Geriatric Patients
6 ADVERSE REACTIONS
7 DRUG INTERACTIONS
7.1 Other Anticholinergic Drugs
7.2 Drugs with Altered Absorption due to Decreased Gastrointestinal Motility and Increased Transit Time
7.3 Gastrointestinal Toxicity with Solid Oral Dosage Forms of Potassium Chloride
8 USE IN SPECIFIC POPULATIONS
8.1 Pregnancy
8.2 Lactation
8.4 Pediatric Use
8.5 Geriatric Use
8.6 Renal Impairment
10 OVERDOSAGE
11 DESCRIPTION
12 CLINICAL PHARMACOLOGY
12.1 Mechanism of Action
12.2 Pharmacodynamics
12.3 Pharmacokinetics
13 NONCLINICAL TOXICOLOGY
13.1 Carcinogenesis & Mutagenesis & Impairment Of Fertility
16 HOW SUPPLIED/STORAGE AND HANDLING
17 PATIENT COUNSELING INFORMATION
- *
- Sections or subsections omitted from the full prescribing information are not listed.
1 INDICATIONS & USAGE
ROBINUL and ROBINUL FORTE are indicated in adults to reduce symptoms of a peptic ulcer as an adjunct to treatment of peptic ulcer.
Limitations of Use
ROBINUL and ROBINUL FORTE are not indicated as monotherapy for the treatment of peptic ulcer because effectiveness in peptic ulcer healing has not been established.
2 DOSAGE & ADMINISTRATION
2.1 Important Dosing Information
• ROBINUL FORTE is not recommended for patients in whom a lower dosage strength of oral glycopyrrolate (e.g., ROBINUL or another 1 mg tablet strength) is appropriate for initial or maintenance treatment because the dosage strength of ROBINUL FORTE may exceed the recommended initial and maintenance dosage of oral glycopyrrolate tablets.
2.2 Recommended Dosage
• The recommended initial dosage of ROBINUL for adults is 1 mg three times daily (in the morning, early afternoon, and at bedtime). Some patients may require 2 mg at bedtime to assure overnight control of symptoms. For maintenance, a dosage of 1 mg twice a day is frequently adequate.
• The recommended dosage of ROBINUL FORTE for adults is 2 mg two or three times daily at equally spaced intervals.
• The maximum recommended daily dosage of glycopyrrolate is 8 mg.
• Use the lowest effective dosage of glycopyrrolate to control symptoms. If patients can be titrated to a lower dose, switch from ROBINUL FORTE to ROBINUL or another 1 mg oral tablet of glycopyrrolate.
3 DOSAGE FORMS & STRENGTHS
4 CONTRAINDICATIONS
ROBINUL and ROBINUL FORTE are contraindicated in:
• Patients at risk for anticholinergic toxicity due to an underlying medical condition, including:
o Glaucoma [see Warnings and Precautions (5.1)]
o Obstructive uropathies, including prostatic hypertrophy
o Mechanical obstructive diseases of the gastrointestinal tract (e.g., pyloroduodenal stenosis, strictures) [see Warnings and Precautions (5.2)]
o Gastrointestinal motility disorders (e.g., achalasia, paralytic ileus, intestinal atony) [see Warnings and Precautions (5.3)]
o Bleeding gastrointestinal ulcer
o Active inflammatory or infectious colitis which can lead to toxic megacolon
o History of or current toxic megacolon
o Myasthenia gravis
• Patients with a hypersensitivity to glycopyrrolate or any of the inactive ingredients in ROBINUL and ROBINUL FORTE [see Adverse Reactions (6) and Description (11)].
5 WARNINGS AND PRECAUTIONS
5.1 Precipitation of Acute Glaucoma
Glycopyrrolate may cause increased intraocular pressure in patients with glaucoma and reduce the effects of antiglaucoma agents. Instruct patients to discontinue ROBINUL and ROBINUL FORTE and promptly seek medical care if they experience symptoms of acute angle-closure glaucoma (pain and reddening of the eyes accompanied by dilated pupils) [see Contraindications (4)].
5.2 Partial or Complete Mechanical Intestinal Obstruction
ROBINUL and ROBINUL FORTE may worsen intestinal mechanical obstruction, and diarrhea may be an early symptom of incomplete intestinal obstruction, especially in patients with ileostomy or colostomy. If partial or complete intestinal obstruction is suspected, discontinue the use of ROBINUL and ROBINUL FORTE and evaluate for potential intestinal obstruction [see Contraindications (4)].
5.3 Gastrointestinal Adverse Reactions Due to Decreased Gastrointestinal Motility
Glycopyrrolate reduces gastrointestinal motility and may result in delayed gastric emptying, constipation, and intestinal pseudo-obstruction and may precipitate or aggravate paralytic ileus and toxic megacolon [see Contraindications (4)]. The risk of gastrointestinal adverse reactions is further increased with the use of other anticholinergics and other medications that decrease gastrointestinal peristalsis.
Monitor patients for symptoms of decreased gastrointestinal motility. Concomitant use of ROBINUL and ROBINUL FORTE and other anticholinergics or other medications that decrease GI peristalsis is not recommended [see Drug Interactions (7.2)].
5.4 Cognitive and Visual Adverse Reactions
Glycopyrrolate may produce drowsiness and blurred vision and impair the mental and/or physical abilities required for the performance of hazardous tasks such as driving a motor vehicle, operating machinery, or performing other hazardous work [see Adverse Reactions (6)]. Concomitant use of other drugs that have anticholinergic properties may increase these effects [see Drug Interactions (7.1)].
Inform patients not to operate motor vehicles or other dangerous machinery or perform other hazardous tasks until they are reasonably certain that ROBINUL and ROBINUL FORTE does not affect them adversely.
Discontinue ROBINUL and ROBINUL FORTE if signs or symptoms of cognitive or visual impairment develop.
5.5 Heat Prostration at High Environmental Temperatures
In the presence of a high environmental temperature, heat prostration resulting in fever and heatstroke can occur with the use of ROBINUL and ROBINUL FORTE due to decreased sweating, particularly in geriatric patients [see Adverse Reactions (6)]. Advise patients to avoid exposure to hot or very warm environmental temperatures when taking ROBINUL and ROBINUL FORTE. ROBINUL and ROBINUL FORTE are not recommended in geriatric patients [see Warnings and Precautions (5.7)].
5.6 Other Conditions Exacerbated by Anticholinergic Adverse Reactions
ROBINUL and ROBINUL FORTE are not recommended in patients with other conditions exacerbated by anticholinergic adverse reactions (e.g., autonomic neuropathy, hyperthyroidism, cardiac disease, and hiatal hernia associated with reflux esophagitis) and in patients taking other anticholinergic medications [see Drug Interactions (7.1)].
5.7 Increased Risk of Anticholinergic Adverse Reactions in Geriatric Patients
Geriatric patients 65 years of age and older are at increased risk of anticholinergic adverse reactions that may lead to complications of urinary retention, bowel obstruction, heat prostration, arrhythmias, delirium, and falls or fractures. ROBINUL and ROBINUL FORTE are not recommended in geriatric patients and may be contraindicated in some geriatric patients with underlying medical conditions [see Contraindications (4),Warnings and Precautions (5.2, 5.5), Adverse Reactions (6) and Use in Specific Populations (8.5)].
6 ADVERSE REACTIONS
The following serious or otherwise important adverse reactions are discussed elsewhere in the labeling:
• Precipitation of Acute Glaucoma [see Warnings and Precautions (5.1)]
• Partial or Complete Mechanical Intestinal Obstruction [see Warnings and Precautions (5.2)]
• Gastrointestinal Adverse Reactions due to Decreased Gastrointestinal Motility [see Warnings and Precautions (5.3)]
• Cognitive and Visual Adverse Reactions [see Warnings and Precautions (5.4)]
• Heat Prostration at High Environmental Temperatures [see Warnings and Precautions (5.5)]
• Other Conditions Exacerbated by Anticholinergic Adverse Reactions [see Warnings and Precautions (5.6)]
• Increased Risk of Anticholinergic Adverse Reactions in Geriatric Patients [see Warnings and Precautions (5.7)]
The following adverse reactions associated with the use of glycopyrrolate, or other anticholinergic drugs, were identified in clinical studies or postmarketing reports. Because some of these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Cardiac Disorders: chest, pain, hypertension, tachycardia
Endocrine Disorders: decreased sweating
Eye Disorders: blurred vision, cycloplegia, dilatation of the pupil, increased ocular tension
Gastrointestinal Disorders: bloated feeling, constipation, dry mouth, dysgeusia, nausea, vomiting
Immune System Disorders: anaphylaxis [see Contraindications (4)]
Nervous System Disorders: agitation, dizziness, drowsiness, headache, insomnia, mental confusion, nervousness, weakness
Respiratory Disorders: respiratory depression, throat irritation
Renal and Urinary Disorders: urinary hesitancy, urinary retention
Reproductive System and Breast Disorders: impotence, suppression of lactation
Vascular Disorders: flushing
7 DRUG INTERACTIONS
7.1 Other Anticholinergic Drugs
There is potential for an additive interaction between glycopyrrolate and concomitantly used anticholinergic drugs (e.g., tricyclic antidepressants, anti-epileptics, class I antiarrhythmics, antispasmodics, amantadine) resulting in increased anticholinergic adverse reactions. Co-administration of antipsychotics with glycopyrrolate may lead to worsening of tardive dyskinesia. ROBINUL and ROBINUL FORTE are not recommended in patients taking other anticholinergic drugs [see Warnings and Precautions (5.3, 5.4, 5.6)].
7.2 Drugs with Altered Absorption due to Decreased Gastrointestinal Motility and Increased Transit Time
Decreased gastrointestinal motility by glycopyrrolate may impact absorption of other drugs leading to increased or decreased drug exposure. ROBINUL and ROBINUL FORTE are not recommended in patients taking other drugs that are affected by altered gastrointestinal motility [see Warnings and Precautions (5.3)].
7.3 Gastrointestinal Toxicity with Solid Oral Dosage Forms of Potassium Chloride
Oral glycopyrrolate may worsen gastrointestinal mucosal injury reported with solid oral dosage forms of potassium chloride due to decreased gastric motility and increased transit time, leading to prolonged contact with the gastrointestinal mucosa. ROBINUL and ROBINUL FORTE are not recommended in patients taking solid oral dosage forms of potassium chloride.
8 USE IN SPECIFIC POPULATIONS
8.1 Pregnancy
Risk Summary
Over decades of use, there is an absence of published data on orally administered glycopyrrolate in pregnant women, including an absence of any reports of a drug-associated risk of major birth defects, miscarriage, or other adverse maternal or fetal outcomes. In animal studies, at non-maternally toxic doses of oral glycopyrrolate, there were no adverse developmental effects in rats or rabbits. A pre- and post-natal development study of oral glycopyrrolate in rats showed a decrease in pup mean bodyweight that recovered post nursing, with no other developmental effects observed (see Data).
The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. 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.
Data
Animal Data
At non-maternally toxic doses of oral glycopyrrolate, there were no effects on embryo-fetal development or toxicity in rats or rabbits. A pre- and post-natal development study of oral glycopyrrolate in rats showed a decrease in pup mean bodyweight that recovered post nursing, with no other developmental effects observed.
In a published reproductive and developmental study, male and female rats were administered glycopyrrolate in the diet at 0 mg/kg/day, 32.5 mg/kg/day, 63 mg/kg/day, and 130 mg/kg/day for 3 weeks to 5 weeks and through up to three consecutive litters. There was no indication of abnormalities in the pups of treated dams. There was a decreased rate of conception and in survival rate at weaning for all treated animals in a dose-related manner. Diminished rates of conception may be due to diminished seminal secretion [see Nonclinical Toxicology (13.1)].
8.2 Lactation
Risk Summary
There are no data on the presence of glycopyrrolate in either human or animal milk, the effects on the breastfed infant, or the effects on milk production. As with other anticholinergic drugs, glycopyrrolate may cause suppression of lactation. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for ROBINUL and ROBINUL FORTE and any potential adverse effects on the breastfed infant from ROBINUL and ROBINUL FORTE.
8.5 Geriatric Use
Geriatric patients 65 years of age and older may be more sensitive to the anticholinergic adverse reactions of glycopyrrolate leading to complications of urinary retention, bowel obstruction, heat prostration, arrhythmias, delirium, and falls or fractures; therefore, ROBINUL and ROBINUL FORTE are not recommended in geriatric patients and may be contraindicated in some geriatric patients with underlying medical conditions [see Contraindications (4) and Warnings and Precautions (5)].
8.6 Renal Impairment
Glycopyrrolate is substantially excreted by the kidney [see Clinical Pharmacology (12.3)].
Monitor patients with renal impairment for anticholinergic adverse reactions [see Adverse Reactions (6)]. If anticholinergic adverse reactions occur, discontinue ROBINUL and ROBINUL FORTE.
10 OVERDOSAGE
Signs and symptoms of glycopyrrolate overdosage are related to excessive anti-muscarinic anticholinergic activity and are generally peripheral (e.g., flushing, hyperthermia, tachycardia, ileus, urinary retention, loss of ocular accommodation, and light sensitivity due to mydriasis), but central nervous system toxicity (agitation, seizures, hyperthermia) may also occur.
If over-exposure occurs, call the Poison Control Center at 1-800-222-1222 for current information on the management of glycopyrrolate poisoning and overdosage.
Management of glycopyrrolate overdosage is based upon presenting signs and symptoms, including close observation for severe or life-threatening complications which may require respiratory and cardiovascular monitoring and support. Consider administration of activated charcoal and/or use of a reversible anticholinesterase as appropriate or recommended by Poison Control.
11 DESCRIPTION
ROBINUL and ROBINUL FORTE tablets contain synthetic anticholinergic glycopyrrolate. Glycopyrrolate is a quaternary ammonium compound with the following chemical name: 3-[(cyclopentyl hydroxyphenylacetyl)oxy]-1,1-dimethylpyrrolidinium bromide. The molecular formula for glycopyrrolate is C19H28BrNO3, the molecular weight is 398.3 g/mol, and the structural formula is:
Each ROBINUL tablet contains glycopyrrolate, USP 1 mg, as the active ingredient. Each ROBINUL FORTE tablet contains glycopyrrolate, USP 2 mg, as the active ingredient. The inactive ingredients are dibasic calcium phosphate, lactose monohydrate, magnesium stearate, povidone, and sodium starch glycolate.
12 CLINICAL PHARMACOLOGY
12.1 Mechanism of Action
Glycopyrrolate, an anticholinergic (antimuscarinic) agent, inhibits the action of acetylcholine on parietal cells in the stomach and decreases the volume and acidity of gastric secretions.
12.2 Pharmacodynamics
No formal pharmacodynamic studies have been conducted with ROBINUL and ROBINUL FORTE.
12.3 Pharmacokinetics
Patients with Renal Impairment
In the published literature, glycopyrrolate 4 mcg/kg was administered intravenously (ROBINUL and ROBINUL FORTE are not recommended for intravenous use) in uremic patients undergoing renal transplantation surgery. The mean AUC (10.6 mcg·h/L) and 24-hour urinary excretion (7%) for glycopyrrolate were significantly different from normal healthy adult subjects undergoing general surgery (3.7 mcg·h/L, and 65%, respectively) [see Use in Specific Populations (8.6)].
13 NONCLINICAL TOXICOLOGY
13.1 Carcinogenesis & Mutagenesis & Impairment Of Fertility
Reproduction studies in rats resulted in diminished rates of conception in a dose-related manner. Studies in dogs suggest that diminished rates of conception may be due to diminished seminal secretion, which is evident at high doses of glycopyrrolate.
16 HOW SUPPLIED/STORAGE AND HANDLING
ROBINUL (glycopyrrolate) tablets, 1 mg are white, round, flat-faced, beveled-edge tablet, debossed “CS” and “007” on one side and functionally scored on the other side. Available as
• Bottles of 30 NDC 70199-007-30
• Bottles of 90 NDC 70199-007-90
ROBINUL FORTE (glycopyrrolate) tablets, 2 mg are white, round, flat-faced, beveled-edge tablet, debossed “CS” score “008” on one side and plain on the other side. Available as
• Bottles of 30 NDC 70199-008-30
• Bottles of 90 NDC 70199-008-90
Store at controlled room temperature, 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature]. Keep out of reach of children.
Dispense in a tight container.
17 PATIENT COUNSELING INFORMATION
Precipitation of Acute Glaucoma
Advise patients to discontinue ROBINUL and ROBINUL FORTE and promptly seek medical care if they experience symptoms of acute angle-closure glaucoma (pain and reddening of the eyes accompanied by dilated pupils) [see Warnings and Precautions (5.1)].
Partial or Complete Mechanical Intestinal Obstruction
Advise patients to contact their healthcare provider if diarrhea occurs, especially in patients with ileostomy or colostomy [see Warnings and Precautions (5.2)].
Gastrointestinal Adverse Reactions Due to Decreased Gastrointestinal Motility
Inform patients that ROBINUL and ROBINUL FORTE may cause adverse reactions related to decreased gastrointestinal motility and report to their healthcare provider if they experience symptoms such as vomiting, early satiety, abdominal distention, and constipation [see Warnings and Precautions (5.3)].
Cognitive and Visual Adverse Reactions
Inform patients that ROBINUL and ROBINUL FORTE may cause cognitive or visual impairment and not operate motor vehicles or other dangerous machinery or perform other hazardous tasks until they are reasonably certain that ROBINUL and ROBINUL FORTE do not affect them adversely. Advise patients to discontinue ROBINUL and ROBINUL FORTE immediately and contact their healthcare provider if symptoms develop (e.g., drowsiness or blurred vision) [see Warnings and Precautions (5.4)].
Heat Prostration at High Environmental Temperatures
Inform patients that ROBINUL and ROBINUL FORTE can reduce sweating, leading to the possibility of heat exhaustion or heat stroke. Advise patients to avoid exposure to hot or very warm environmental temperatures [see Warnings and Precautions (5.5)].
Manufactured for:
Casper Pharma LLC
East Brunswick, NJ 08816
Manufactured by:
Suven Pharmaceuticals Limited,
Telangana, India
M.L.No.: 24/MD/AP/2009/F/CC
Revised: 09/2022
PIB00890-05
ROBINUL® and ROBINUL FORTE® are registered trademarks of CASPER PHARMA LLC.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
| ROBINUL
glycopyrrolate tablet |
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| ROBINUL FORTE
glycopyrrolate tablet |
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| Labeler - Casper Pharma LLC (080025838) |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Suven Pharmaceuticals Limited | 677604288 | ANALYSIS(70199-007, 70199-008) , API MANUFACTURE(70199-007) , LABEL(70199-007, 70199-008) , MANUFACTURE(70199-007, 70199-008) , PACK(70199-007, 70199-008) | |