NDC 60219-1502 – Phenoxybenzamine hydrochloride

Phenoxybenzamine Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC60219-1502

Product details

Brand name
Phenoxybenzamine hydrochloride
Generic name
Phenoxybenzamine hydrochloride
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA212568
Marketed since
October 30, 2020
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Phenoxybenzamine hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
60219-1502-1100 CAPSULE in 1 BOTTLE (60219-1502-1)Oct 30, 2020

Recalls mentioning this NDC

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