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Isuprel
Isuprel - 52584-021-01 - (Isuprel)
Drug Information of Isuprel
| Product NDC: | 52584-021 |
| Proprietary Name: | Isuprel |
| Non Proprietary Name: | Isuprel |
| Active Ingredient(s): | .2 mg/mL & nbsp; Isuprel |
| Administration Route(s): | INTRACARDIAC; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Isuprel
| Product NDC: | 52584-021 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA010515 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100301 |
Package Information of Isuprel
| Package NDC: | 52584-021-01 |
| Package Description: | 1 AMPULE in 1 BAG (52584-021-01) > 1 mL in 1 AMPULE |
NDC Information of Isuprel
| NDC Code | 52584-021-01 |
| Proprietary Name | Isuprel |
| Package Description | 1 AMPULE in 1 BAG (52584-021-01) > 1 mL in 1 AMPULE |
| Product NDC | 52584-021 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isuprel |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRACARDIAC; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20100301 |
| Marketing Category Name | NDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | ISOPROTERENOL HYDROCHLORIDE |
| Strength Number | .2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC] |
