DIBUCAINE
- Product NDC
- 81266-920
- 11-digit product format
- 812660920
- Labeler code
- 81266
- Product ID
- 81266-920_b6ca4519-6c8f-49e0-e053-2995a90af800
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIBUCAINE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- NUGERI LLC
- Application
- part346
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-05-01
- Marketing end
- 0000-00-00
- Substance
- DIBUCAINE
- Active strength
- 0 g/g
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81266-920-01 | 81266092001 | 28 g in 1 TUBE (81266-920-01) | 28 g | 2021-05-01 | 0000-00-00 | No | No | Current |