NDC 55150-112 – Ampicillin

Ampicillin Sodium 500 mg/1 · Injection, Powder, For Solution · Intramuscular, Intravenous

Human Prescription Drug 1 recall

Product NDC55150-112

Product details

Brand name
Ampicillin
Generic name
Ampicillin Sodium
Labeler
Eugia US LLC
Dosage form
Injection, Powder, For Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA065499
Marketed since
February 1, 2012
Listing expires
December 31, 2026
Pharmacologic class
Penicillin-class Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ampicillin →

Package NDC codes (1)

Package NDCDescriptionSince
55150-112-1010 VIAL in 1 BOX (55150-112-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIALFeb 1, 2012

Recalls mentioning this NDC

Other Ampicillin products