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
- 83270-314_519efe7d-db24-3b5e-e063-6394a90a427d
- Product NDC
- 83270-314
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- Ampicillin
- Labeler
- ONESOURCE SPECIALTY PHARMA LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260227
- Source listing expiry
- 20271231
Source-listed ingredients
- AMPICILLIN SODIUM — 2 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (83270-314-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL · 83270-314-10
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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