| Product NDC: | 0409-3073 |
| Proprietary Name: | Ephedrine |
| Non Proprietary Name: | EPHEDRINE SULFATE |
| Active Ingredient(s): | 50 mg/mL & nbsp; EPHEDRINE SULFATE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0409-3073 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20050908 |
| Package NDC: | 0409-3073-31 |
| Package Description: | 10 AMPULE in 1 CARTON (0409-3073-31) > 1 mL in 1 AMPULE |
| NDC Code | 0409-3073-31 |
| Proprietary Name | Ephedrine |
| Package Description | 10 AMPULE in 1 CARTON (0409-3073-31) > 1 mL in 1 AMPULE |
| Product NDC | 0409-3073 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | EPHEDRINE SULFATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20050908 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Hospira, Inc. |
| Substance Name | EPHEDRINE SULFATE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |