Indications and uses
For use as adjunctive therapy in the treatment of peptic ulcer.
For use as adjunctive therapy in the treatment of peptic ulcer.
The dosage of Glycopyrrolate Tablets, USP should be adjusted to the needs of the individual patient to assure symptomatic controlwith a minimum of adverse reactions. The presently recommended maximum daily dosage of glycopyrrolate is 8 mg. The recommended initial dosage of Glycopyrrolate 1 mg tablets for adults is one tablet three times daily (in the morning, early afternoon, and at bedtime). Some patients may req...
Glycopyrrolate Tablets, USP 1.5 mg contains the synthetic anticholinergic, glycopyrrolate. Glycopyrrolate is a quaternary ammonium compound with the following chemical name: 3-[(cyclopentylhydroxyacetyl) oxy]-1,1-dimethylpyrrolidinium bromide.
C19H28BrNO3 MW: 398.33
Each tablet contains:
Glycopyrrolate, USP.................... 1.5 mg
Inactive Ingredients: Dibasic Calcium Phosphate, Anhydrous Lactose, Magnesium Stearate, Povidone, Sodium Starch Glycolate.
Glycopyrrolate, like other anticholinergic (antimuscarinic) agents, inhibits the action of acetylcholine on structures innervated by postganglionic cholinergic nerves and on smooth muscles that respond to acetylcholine by lack cholinergic innervation. These peripheral cholinergic receptors are present in the autonomic effector cells of smooth muscle, cardiac muscle, the sino-atrial node, the atrioventricular node, exocrine glands, and, to a limited degree, in the autonomic ganglia. Thus, it diminishes the volume and free acidity of gastric secretions and controls excessive pharyngeal, tracheal, and bronchial secretions.
Glycopyrrolate antagonizes muscarinic symptoms (e.g., bronchorrhea, bronchospasm, bradycardia, and intestinal hypermotility) induced by cholinergic drugs such as the anticholinesterases.
The highly polar quaternary ammonium group of glycopyrrolate limits its passage across lipid membranes, such as the blood-brain barrier, in contrast to atropine sulfate and scopolamine hydrobromide, which are non-polar tertiary amines which penetrate lipid barriers easily.
For use as adjunctive therapy in the treatment of peptic ulcer.
Glaucoma; obstructive uropathy (for example, bladder neck obstruction due to prostatic hypertrophy); obstructive disease of the gastrointestinal tract (as in achalasia, pyloroduodenal stenosis, etc.); paralytic ileus; intestinal atony of the elderly or debilitated patient; unstable cardiovascular status in acute hemorrhage; severe ulcerative colitis; toxic megacolon complicating ulcerative colitis; myasthenia gravis. Glycopyrrolate tablets are contraindicated in those patients with a hypersensitivity to glycopyrrolate.
In the presence of a high environmental temperature, heat prostration (fever and heat stroke due to decreased sweating) can occur with the use of Glycopyrrolate Tablets, USP.
Diarrhea may be an early symptom of incomplete intestinal obstruction, especially in patients with ileostomy or colostomy. In this instance treatment with this drug would be inappropriate and possibly harmful.
Glycopyrrolate Tablets, USP may produce drowsiness or blurred vision. In this event, the patient should be warned not to engage in activities requiring mental alertness such as operating a motor vehicle or other machinery, or performing hazardous work while taking this drug.
Theoretically, with overdosage, a curare-like action may occur, i.e., neuromuscular blockade leading to muscular weakness and possible paralysis.
Use Glycopyrrolate Tablets, USP with caution in the elderly and in all patients with:
There are no known drug interactions.
The safety of this drug during pregnancy has not been established. The use of any drug during pregnancy requires that the potential benefits of the drug be weighed against possible hazards to mother and child. Reproduction studies in rats revealed no teratogenic effects from glycopyrrolate; however, the potent anticholinergic action of this agent resulted in diminished rates of conception and of survival at weaning, in a dose-related manner. Other studies in dogs suggest that this may be due to diminished seminal secretion which is evident at high doses of glycopyrrolate. Information on possible adverse effects in the pregnant female is limited to uncontrolled data derived from marketing experience. Such experience has revealed no reports of teratogenic or other fetus-damaging potential. No controlled studies to establish the safety of the drug in pregnancy have been performed.
It is not known whether this drug is excreted in human milk. As a general rule, nursing should not be undertaken while a patient is on a drug since many drugs are excreted in human milk.
Since there is no adequate experience in pediatric patients who have received this drug, safety and efficacy in pediatric patients have not been established.
Anticholinergics produce certain effects, most of which are extensions of their fundamental pharmacological actions. Adverse reactions to anticholinergics in general may include xerostomia; decreased sweating; urinary hesitancy and retention; blurred vision; tachycardia; palpitations; dilation of the pupil; cycloplegia; increased ocular tension; loss of taste; headaches; nervousness; mental confusion; drowsiness; weakness; dizziness; insomnia; nausea; vomiting; constipation; bloated feeling; impotence; suppression of lactation; severe allergic reaction or drug idiosyncrasies including anaphylaxis, urticaria and other dermal manifestations.
Glycopyrrolate Tablets, USP is chemically a quaternary ammonium compound; hence, its passage across lipid membranes, such as the blood-brain barrier, is limited in contrast to atropine sulfate and scopolamine hydrobromide. For this reason the occurrence of CNS related side effects is lower, in comparison to their incidence following administration of anticholinergics which are chemically tertiary amines that can cross this barrier readily.
Call your doctor for medical advice about side effects.
To report SUSPECTED ADVERSE REACTIONS, contact the FDA at 1-800-FDA-1088 or
www.fda.gov/medwatch
The symptoms of overdosage of glycopyrrolate are peripheral in nature rather than central.
The dosage of Glycopyrrolate Tablets, USP should be adjusted to the needs of the individual patient to assure symptomatic controlwith a minimum of adverse reactions. The presently recommended maximum daily dosage of glycopyrrolate is 8 mg.
The recommended initial dosage of Glycopyrrolate 1 mg tablets for adults is one tablet three times daily (in the morning, early afternoon, and at bedtime). Some patients may require two tablets at bedtime to assure overnight control of symptoms.
For maintenance, a dosage of one tablet twice a day is frequently adequate.
The recommended dosage of Glycopyrrolate 2 mg tablets for adults is one tablet two or three times daily at equally spaced intervals.
The Glycopyrrolate 1.5 mg tablets may be used to provide intermediate titration doses based on response of the patient.
Glycopyrrolate Tablets, USP are not recommended for use in pediatric patients under the age of 12 years.
Glycopyrrolate Tablets, USP 1.5 mg are compressed white tablets debossed GP on one side and 1.5 on the other and are supplied in bottles of 30 (72887-160-03).
Store at 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 tight, light-resistant container, as defined in the USP, using a child-resistant closure.
Rx Only
Distributed by:
FH2 Pharma LLC
Delray Beach, FL 33444
Revised: 08/2021
| Class | Version | Type | Effective |
|---|---|---|---|
| GLYCOPYRRONIUM Pharmacologic Class Indexing | 4 | Indexing - Pharmacologic Class | 20231113 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 138c3de2-4b03-4255-92b5-f022482d81bc | Product name | 4 | 20260113 |
| 4dc252b1-bb5f-8bb6-4fa8-f3a45efd810e | Product name | 5 | 20250304 |
| f58f10d3-5fa9-4c2e-9a6e-77029e9ed80b | Product name | 1 | 20231002 |
| 76dcac30-469f-4f92-9c55-70950d209446 | Product name | 1 | 20230809 |
| 132196a6-5117-4b6e-a9dd-27f2793580c6 | Product name | 1 | 20230112 |
| ac1f888b-a1db-4d2e-abbc-973f21c2ce1b | Product name | 1 | 20220720 |
| d84dd569-7bf0-1410-25eb-017ef37dd406 | Product name | 9 | 20210902 |
| 7d8c8d5a-f174-4e6b-97b1-6fd615c5df9a | Product name | 1 | 20210204 |
| 58b12de9-b891-41c7-9be6-ff47de5ec28b | Product name | 1 | 20180828 |
| 9aff7b10-8e47-4b10-9a92-803440a37ce2 | Product name | 1 | 20180206 |
| ce066c73-ca6f-49fc-83d4-d3cf6728e8a1 | Product name | 1 | 20160616 |
| fb29b8a9-c2d0-42bb-aea8-9bc2a87db75a | Product name | 1 | 20151113 |
| ab7ba50c-5a47-47e6-8dd6-fa32a52559f6 | Product name | 1 | 20151109 |
| 29ae08d1-069f-9822-4820-152d5dc67797 | Product name | 1 | 20140508 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72887-160-03 | GLYCOPYRROLATE | 30 in 1 BOTTLE | TABLET | 30 | 3 |
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72887-160-03 | EA - Each | 72887-160 | 4c4a2600-ae1e-44f2-b0e7-b5e81fec1d2a | 1 | 2022-04-06 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72887-160 | 72887-160-03 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCOPYRROLATE | V92SO9WP2I | ACTIB |
| CALCIUM PYROPHOSPHATE | X69NU20D19 | IACT |
| ANHYDROUS LACTOSE | 3SY5LH9PMK | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| POVIDONE, UNSPECIFIED | FZ989GH94E | IACT |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | 5856J3G2A2 | IACT |
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A091522-001 | GLYCOPYRROLATE | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 |
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-09-14 22:38:34 | 2026-08 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | 84e616aacf4f… | |
| 2026-08-18 06:07:40 | 2026-07 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | caaa826d4ba7… | |
| 2026-02-19 14:30 UTC | 2026-02 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | 011fe1cb6892… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | 31067a03dcf5… | |
| 2025-08-23 18:47 UTC | 2025-08 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | 6a471c1ec25d… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | fd3edfee7708… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | b8a1b40f171c… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | 03ed91905a0d… | |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | 2680178bc6a6… | |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | 5bbf6a4d5a75… | |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | d8e5a09893c0… | |
| 2024-10-29 15:01 UTC | 2024-10 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | d06236e962d9… | |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | RS | 2012-03-12 | 79d66fd596c7… | |
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 301d65b070ca… | ||
| 2024-06-18 03:08 UTC · 5 captures of this ZIP | 2024-06 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 1e350fbaab3a… | ||
| 2024-05-31 18:47 UTC | 2024-05 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 8072bd15b7f6… | ||
| 2022-06-29 02:47 UTC · 2 captures of this ZIP | 2022-06 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 5c6f7cd8ea54… | ||
| 2022-04-08 23:34 UTC | 2022-04 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 5d02ea3f76ae… | ||
| 2022-04-04 05:41 UTC | 2022-04 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 4b0b4de00fa7… | ||
| 2019-12-13 00:20 UTC | 2019-12 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 74a2ff9319b5… | ||
| 2022-03-09 01:35 UTC | 2022-03 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | bb7c543d1eb4… | ||
| 2021-12-28 21:50 UTC | 2021-12 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 782e0a99824c… | ||
| 2021-05-05 16:15 UTC · 3 captures of this ZIP | 2021-05 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 87673890dc5c… | ||
| 2021-03-12 10:30 UTC | 2021-03 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 5aa47cf7b7d7… | ||
| 2020-12-22 03:56 UTC | 2020-12 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 8869cabd3fbd… | ||
| 2020-11-12 02:37 UTC | 2020-11 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | c0c555d07b60… | ||
| 2019-12-14 00:12 UTC | 2019-12 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 3f01610625f2… | ||
| 2019-09-15 20:21 UTC | 2019-09 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | b00525d2431f… | ||
| 2019-07-19 19:46 UTC | 2019-07 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | ea99ee380514… | ||
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 6a51e52b5d6a… | ||
| 2024-02-18 07:12 UTC | 2024-02 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 1c564ffb4f44… | ||
| 2023-12-20 04:57 UTC | 2023-12 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | ea1830bbd6c7… | ||
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | a72a2bbeb626… | ||
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 9b2671bbb829… | ||
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | a67488948f0b… | ||
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 3f0d92c62455… | ||
| 2023-05-13 08:27 UTC | 2023-05 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 053a50430f4f… | ||
| 2023-01-26 05:58 UTC | 2023-01 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 3bdfa0b2c4d7… | ||
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | 3a93d1ddd44b… | ||
| 2022-10-28 04:53 UTC | 2022-10 | A091522-001 | GLYCOPYRROLATE | 1.5MG | TABLET / ORAL | 2012-03-12 | f41ea6bd6efb… |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| GLYCOPYRROLATE | GLYCOPYRROLATE | FH2 Pharma LLC | 18ca98ed-522d-470f-bb22-908bbd7d489a | 2023-12-31 | Warnings, Adverse reactions | 72887-160-03 72887-160 72887016003 5bc26249-4e9b-4870-a696-99779c90dc27 18ca98ed-522d-470f-bb22-908bbd7d489a |
Adverse event summaries are temporarily unavailable. Other product information remains available.