United States · FDA National Drug Code directory
AMPICILLIN
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 23155-914_65071c52-ece6-4774-a50f-ce981776b5e6
- Product NDC
- 23155-914
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- Ampicillin Injection
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250131
- Source listing expiry
- 20261231
Source-listed ingredients
- AMPICILLIN SODIUM — 250 mg/250mg
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 PACKAGE (23155-914-41) / 250 mg in 1 VIAL (23155-914-31) · 23155-914-41
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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