NDC 25021-315 – Phenylephrine Hydrochloride

Phenylephrine Hydrochloride 10 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC25021-315

Product details

Brand name
Phenylephrine Hydrochloride
Generic name
Phenylephrine Hydrochloride
Labeler
Sagent Pharmaceuticals
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA209967
Marketed since
October 15, 2020
Listing expires
December 31, 2026
Pharmacologic class
alpha-1 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Phenylephrine Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
25021-315-0125 VIAL in 1 CARTON (25021-315-01) / 1 mL in 1 VIALOct 15, 2020
25021-315-981 VIAL in 1 CARTON (25021-315-98) / 10 mL in 1 VIALOct 15, 2020
25021-315-9910 VIAL in 1 CARTON (25021-315-99) / 5 mL in 1 VIALOct 15, 2020

Recalls mentioning this NDC

Other Phenylephrine Hydrochloride products