NDC 70069-812 – Phenylephrine Hydrochloride
Phenylephrine Hydrochloride 50 mg/5mL · Injection · Intravenous
Product NDC70069-812
Product details
- Brand name
- Phenylephrine Hydrochloride
- Generic name
- Phenylephrine Hydrochloride
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- Injection
- Route
- Intravenous
- Marketing category
- ANDA · ANDA213318
- Marketed since
- July 17, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-1 Adrenergic Agonist
Active ingredients
- Phenylephrine Hydrochloride 50 mg/5mL
Uses, dosage, side effects and warnings for Phenylephrine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70069-812-10 | 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70069-812-10) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (70069-812-01) | Jul 17, 2023 |
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