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
- 67777-116_275e9fdf-28d0-498a-e063-6294a90a7eea
- Product NDC
- 67777-116
- Form
- OINTMENT
- Composition / generic term
- Bacitracin
- Labeler
- Dynarex Corporation
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20160912
- Source listing expiry
- 20261231
Source-listed ingredients
- BACITRACIN — 500 [USP'U]/1000mg
These values do not establish equivalence or a dose recommendation.
Packages
- 1728 BOX in 1 CASE (67777-116-10) / 144 PACKET in 1 BOX (67777-116-11) / 900 mg in 1 PACKET · 67777-116-10
- 72 TUBE in 1 CASE (67777-116-20) / 14000 mg in 1 TUBE (67777-116-21) · 67777-116-20
- 72 BOX in 1 CASE (67777-116-30) / 1 TUBE in 1 BOX (67777-116-31) / 28400 mg in 1 TUBE · 67777-116-30
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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