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Ephedrine Sulfate
Ephedrine Sulfate - 17478-823-01 - (Ephedrine Sulfate)
Drug Information of Ephedrine Sulfate
| Product NDC: | 17478-823 |
| Proprietary Name: | Ephedrine Sulfate |
| Non Proprietary Name: | Ephedrine Sulfate |
| Active Ingredient(s): | 50 mg/mL & nbsp; Ephedrine Sulfate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ephedrine Sulfate
| Product NDC: | 17478-823 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120311 |
Package Information of Ephedrine Sulfate
| Package NDC: | 17478-823-01 |
| Package Description: | 10 AMPULE in 1 CARTON (17478-823-01) > 1 mL in 1 AMPULE |
NDC Information of Ephedrine Sulfate
| NDC Code | 17478-823-01 |
| Proprietary Name | Ephedrine Sulfate |
| Package Description | 10 AMPULE in 1 CARTON (17478-823-01) > 1 mL in 1 AMPULE |
| Product NDC | 17478-823 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ephedrine Sulfate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20120311 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Akorn, Inc. |
| Substance Name | EPHEDRINE SULFATE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
