NDC Code | 55150-317-10 |
Package Description | 10 AMPULE in 1 CARTON (55150-317-10) / 5 mL in 1 AMPULE (55150-317-01) |
Product NDC | 55150-317 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Isoproterenol Hydrochloride |
Non-Proprietary Name | Isoproterenol Hydrochloride |
Dosage Form | INJECTION, SOLUTION |
Usage | INTRACARDIAC; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20210209 |
Marketing Category Name | ANDA |
Application Number | ANDA211864 |
Manufacturer | Eugia US LLC |
Substance Name | ISOPROTERENOL HYDROCHLORIDE |
Strength | 1 |
Strength Unit | mg/5mL |
Pharmacy Classes | Adrenergic beta-Agonists [MoA], beta-Adrenergic Agonist [EPC] |