Phenylephrine Hydrochloride 00781-3422
Product NDC
00781-3422- Manufacturer
- Sandoz Inc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- September 5, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA208905
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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, SINGLE-DOSE in 1 CARTON (0781-3422-92) / 1 mL in 1 VIAL, SINGLE-DOSE (0781-3422-71)