GLYCOPYRROLATE
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- GLYCOPYRROLATE
- Generic name
- GLYCOPYRROLATE
- Manufacturer
- Solco Healthcare US, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 2972f22e-378c-450b-8869-1354a9bd0ffc
- SPL ID
- 8a403c54-3e23-41fc-bf80-c40e8d867aa2
- Version
- 3
- Effective date
- 2025-11-30
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:57
| Harmonized routes |
|---|
| INTRAMUSCULAR, INTRAVENOUS |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 210927 | derived:openfda.application_number |
| application number | ANDA210927 | openfda.application_number | |
| brand name | GLYCOPYRROLATE | openfda.brand_name | |
| generic name | GLYCOPYRROLATE | openfda.generic_name | |
| manufacturer name | Solco Healthcare US, LLC | openfda.manufacturer_name | |
| ndc | package | 43547-639-25 | openfda.package_ndc |
| ndc | package | 43547-640-01 | openfda.package_ndc |
| ndc | package | 43547-639-01 | openfda.package_ndc |
| ndc | package | 43547-640-25 | openfda.package_ndc |
| ndc | product | 43547-640 | openfda.product_ndc |
| ndc | product | 43547-639 | openfda.product_ndc |
| ndc11 | package | 43547063901 | derived:openfda.package_ndc |
| ndc11 | package | 43547064025 | derived:openfda.package_ndc |
| ndc11 | package | 43547063925 | derived:openfda.package_ndc |
| ndc11 | package | 43547064001 | derived:openfda.package_ndc |
| rxcui | 1731582 | openfda.rxcui | |
| rxcui | 1731590 | openfda.rxcui | |
| spl id | 8a403c54-3e23-41fc-bf80-c40e8d867aa2 | id | |
| spl set id | 2972f22e-378c-450b-8869-1354a9bd0ffc | set_id | |
| unii | V92SO9WP2I | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS This drug should be used with great caution, if at all, in patients with glaucoma. Glycopyrrolate injection may produce drowsiness or blurred vision. The patient should be cautioned regarding activities requiring mental alertness such as operating a motor vehicle or other machinery or performing hazardous work while taking this drug. In addition, in the presence of fever, high environmental temperature and/or during physical exercise, heat prostration can occur with use of anticholinergic agents including glycopyrrolate (due to decreased sweating), particularly in children and the elderly. Diarrhea may be an early symptom of incomplete intestinal obstruction, especially in patients with ileostomy or colostomy. In this instance treatment with glycopyrrolate injection would be inappropriate and possibly harmful.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Anticholinergics, including glycopyrrolate injection, can produce certain effects, most of which are extensions of their pharmacologic actions. Adverse reactions may include xerostomia (dry mouth); urinary hesitancy and retention; blurred vision and photophobia due to mydriasis (dilation of the pupil); cycloplegia; increased ocular tension; tachycardia; palpitation; decreased sweating; loss of taste; headache; nervousness; drowsiness; weakness; dizziness; insomnia; nausea; vomiting; impotence; suppression of lactation; constipation; bloated feeling; severe allergic reactions including anaphylactic/anaphylactoid reactions; hypersensitivity; urticaria, pruritus, dry skin, and other dermal manifestations; some degree of mental confusion and/or excitement, especially in elderly persons. In addition, the following adverse events have been reported from post-marketing experience with glycopyrrolate: malignant hyperthermia; cardiac arrhythmias (including bradycardia, ventricular tachycardia, ventricular fibrillation); cardiac arrest; hypertension; hypotension; seizures; and respiratory arrest. Post-marketing reports have included cases of heart block and QTc interval prolongation associated with the combined use of glycopyrrolate and an anticholinesterase. Injection site reactions including pruritus, edema, erythema, and pain have also been reported. Glycopyrrolate 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.