NDC 65219-014 – Ampicillin

Ampicillin Sodium 250 mg/1 · Injection, Powder, For Solution · Intramuscular, Intravenous

Human Prescription Drug

Product NDC65219-014

Product details

Brand name
Ampicillin
Generic name
Ampicillin sodium
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Powder, For Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA062719
Marketed since
October 30, 2019
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
65219-014-1010 VIAL in 1 CARTON (65219-014-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (65219-014-01)Oct 30, 2019

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