Phenylephrine Hydrochloride 71839-0129
Product NDC
71839-0129- Manufacturer
- Be Pharmaceuticals Inc.
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 10, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA217521
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Phenylephrine Hydrochloride | 10 mg/mL |
Drug Class
Adrenergic alpha1-Agonists [MoA]alpha-1 Adrenergic Agonist [EPC]
Packaging Options(1)
10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (71839-129-10) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE (71839-129-01)