United States · FDA National Drug Code directory
Ampicillin and Sulbactam
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
- 72603-335_c9fe0e6e-db1d-49ec-a16b-aa1de5ae7d5a
- Product NDC
- 72603-335
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- Ampicillin sodium and Sulbactam sodium
- Labeler
- NorthStar Rx, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240301
- Source listing expiry
- 20261231
Source-listed ingredients
- AMPICILLIN SODIUM — 2 g/1
- SULBACTAM SODIUM — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (72603-335-01) · 72603-335-01
- 10 VIAL, SINGLE-DOSE in 1 CARTON (72603-335-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE · 72603-335-10
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 →