NDC 0781-3402 – Ampicillin

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

Human Prescription Drug 1 recall

Product NDC0781-3402

Product details

Brand name
Ampicillin
Generic name
Ampicillin sodium
Labeler
Sandoz Inc
Dosage form
Injection, Powder, For Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA061395
Marketed since
March 3, 1971
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
0781-3402-9510 VIAL, GLASS in 1 PACKAGE (0781-3402-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-3402-78)Mar 3, 1971

Recalls mentioning this NDC

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