Details for New Drug Application (NDA): 214579
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The generic ingredient in EPHEDRINE SULFATE is ephedrine sulfate. There are sixty-eight drug master file entries for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the ephedrine sulfate profile page.
Summary for 214579
Tradename: | EPHEDRINE SULFATE |
Applicant: | Eugia Pharma |
Ingredient: | ephedrine sulfate |
Patents: | 0 |
Pharmacology for NDA: 214579
Mechanism of Action | Adrenergic alpha-Agonists Adrenergic beta-Agonists |
Physiological Effect | Increased Norepinephrine Activity |
Medical Subject Heading (MeSH) Categories for 214579
Suppliers and Packaging for NDA: 214579
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
EPHEDRINE SULFATE | ephedrine sulfate | SOLUTION;INTRAVENOUS | 214579 | ANDA | Eugia US LLC | 55150-373 | 55150-373-25 | 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-373-25) / 1 mL in 1 VIAL, SINGLE-DOSE (55150-373-01) |
EPHEDRINE SULFATE | ephedrine sulfate | SOLUTION;INTRAVENOUS | 214579 | ANDA | Medical Purchasing Solutions, LLC | 71872-7276 | 71872-7276-1 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7276-1) / 1 mL in 1 VIAL, SINGLE-DOSE |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 50MG/ML (50MG/ML) | ||||
Approval Date: | Jun 14, 2021 | TE: | AP | RLD: | No |
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