Details for New Drug Application (NDA): 210333
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The generic ingredient in PHENYLEPHRINE HYDROCHLORIDE is phenylephrine hydrochloride; promethazine hydrochloride. There are twenty-one drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the phenylephrine hydrochloride; promethazine hydrochloride profile page.
Summary for 210333
Tradename: | PHENYLEPHRINE HYDROCHLORIDE |
Applicant: | Meitheal |
Ingredient: | phenylephrine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 210333
Mechanism of Action | Adrenergic alpha1-Agonists |
Medical Subject Heading (MeSH) Categories for 210333
Suppliers and Packaging for NDA: 210333
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PHENYLEPHRINE HYDROCHLORIDE | phenylephrine hydrochloride | SOLUTION;INTRAVENOUS | 210333 | ANDA | Meitheal Pharmaceuticals Inc. | 71288-808 | 71288-808-76 | 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (71288-808-76) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (71288-808-75) |
PHENYLEPHRINE HYDROCHLORIDE | phenylephrine hydrochloride | SOLUTION;INTRAVENOUS | 210333 | ANDA | Meitheal Pharmaceuticals Inc. | 71288-808 | 71288-808-77 | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (71288-808-77) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 50MG/5ML (10MG/ML) | ||||
Approval Date: | Apr 27, 2018 | TE: | AP1 | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 100MG/10ML (10MG/ML) | ||||
Approval Date: | Apr 27, 2018 | TE: | AP1 | RLD: | No |
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