United States · FDA National Drug Code directory
BACITRACIN
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
- 41250-844_ea14c5e8-448a-4f96-b00c-388c2cd3e2d7
- Product NDC
- 41250-844
- Form
- OINTMENT
- Composition / generic term
- Bacitracin
- Labeler
- Meijer Distribution Inc
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20181024
- Source listing expiry
- 20261231
Source-listed ingredients
- BACITRACIN — 500 [USP'U]/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (41250-844-64) / 28 g in 1 TUBE · 41250-844-64
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 →