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
- 71872-7086_fc600b6f-0ddf-10ff-e053-6394a90a6ba5
- Product NDC
- 71872-7086
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- Ampicillin Sodium
- Labeler
- Medical Purchasing Solutions, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120201
- Source listing expiry
- 20261231
Source-listed ingredients
- AMPICILLIN SODIUM — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 BAG (71872-7086-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL · 71872-7086-1
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →