Home
>
National Drug Code (NDC)
>
Ephedrine Sulfate
Ephedrine Sulfate - 66758-008-02 - (Ephedrine Sulfate)
Drug Information of Ephedrine Sulfate
| Product NDC: | 66758-008 |
| 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, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ephedrine Sulfate
| Product NDC: | 66758-008 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20040326 |
Package Information of Ephedrine Sulfate
| Package NDC: | 66758-008-02 |
| Package Description: | 25 VIAL in 1 CARTON (66758-008-02) > 1 mL in 1 VIAL (66758-008-01) |
NDC Information of Ephedrine Sulfate
| NDC Code | 66758-008-02 |
| Proprietary Name | Ephedrine Sulfate |
| Package Description | 25 VIAL in 1 CARTON (66758-008-02) > 1 mL in 1 VIAL (66758-008-01) |
| Product NDC | 66758-008 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ephedrine Sulfate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20040326 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Sandoz Inc |
| Substance Name | EPHEDRINE SULFATE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
