Details for New Drug Application (NDA): 218412
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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 218412
Tradename: | PHENYLEPHRINE HYDROCHLORIDE |
Applicant: | Hainan Poly |
Ingredient: | phenylephrine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 218412
Mechanism of Action | Adrenergic alpha1-Agonists |
Medical Subject Heading (MeSH) Categories for 218412
Suppliers and Packaging for NDA: 218412
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PHENYLEPHRINE HYDROCHLORIDE | phenylephrine hydrochloride | SOLUTION;INTRAVENOUS | 218412 | ANDA | Hainan Poly Pharm. Co., Ltd. | 14335-440 | 14335-440-01 | 25 VIAL, SINGLE-DOSE in 1 CARTON (14335-440-01) / 1 mL in 1 VIAL, SINGLE-DOSE |
PHENYLEPHRINE HYDROCHLORIDE | phenylephrine hydrochloride | SOLUTION;INTRAVENOUS | 218412 | ANDA | Hainan Poly Pharm. Co., Ltd. | 14335-441 | 14335-441-01 | 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (14335-441-01) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | SOLUTION;INTRAVENOUS | Strength | 10MG/ML (10MG/ML) | ||||
Approval Date: | Mar 14, 2024 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | SOLUTION;INTRAVENOUS | Strength | 50MG/5ML (10MG/ML) | ||||
Approval Date: | Mar 14, 2024 | TE: | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | DISCN | Dosage: | SOLUTION;INTRAVENOUS | Strength | 100MG/10ML (10MG/ML) | ||||
Approval Date: | Mar 14, 2024 | TE: | RLD: | No |
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