Phenylephrine Hydrochloride 70069-0801
Product NDC
70069-0801- Manufacturer
- Somerset Therapeutics, Llc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- September 22, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA213318
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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)
25 VIAL in 1 CARTON (70069-801-25) / 1 mL in 1 VIAL (70069-801-01)