United States · FDA National Drug Code directory
tobramycin
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
- 70436-110_4a830833-6027-9c0a-e063-6394a90a27ee
- Product NDC
- 70436-110
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- tobramycin
- Labeler
- Slate Run Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230201
- Source listing expiry
- 20271231
Source-listed ingredients
- TOBRAMYCIN — 1200 mg/30mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 VIAL (70436-110-36) · 70436-110-36
- 180 mL in 1 CARTON (70436-110-56) · 70436-110-56
- 30 mL in 1 CARTON (70436-110-80) · 70436-110-80
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 →