antibiotic
- Product NDC
- 41250-536
- 11-digit product format
- 412500536
- Labeler code
- 41250
- Product ID
- 41250-536_4c57de5f-3623-45d7-9779-989fa6ce8e94
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bacitracin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Meijer Distribution Inc
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-04-15
- Marketing end
- 0000-00-00
- Substance
- BACITRACIN
- Active strength
- 500 [USP'U]/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record