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
- 68001-477_097d4e93-7f8a-53f8-e063-6294a90a4e40
- Product NDC
- 68001-477
- Form
- OINTMENT
- Composition / generic term
- Bacitracin
- Labeler
- BluePoint Laboratories
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20201124
- Source listing expiry
- 20261231
Source-listed ingredients
- BACITRACIN — 500 [iU]/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (68001-477-46) / 14.2 g in 1 TUBE · 68001-477-46
- 1 TUBE in 1 CARTON (68001-477-47) / 28.4 g in 1 TUBE · 68001-477-47
- 1 PACKET in 1 CARTON (68001-477-48) / .9 g in 1 PACKET (68001-477-45) · 68001-477-48
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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