Ellzia Pak
- Product NDC
- 59088-846
- 11-digit product format
- 590880846
- Labeler code
- 59088
- Product ID
- 59088-846_b3d87a64-a63b-f6b6-e053-2995a90a807d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- triamcinolone acetonide, dimethicone
- Dosage form
- KIT
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-12-29
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 59088-846-00 | 59088084600 | 1 KIT in 1 CARTON (59088-846-00) * 80 g in 1 TUBE (52565-014-80) * 118 mL in 1 TUBE (59088-333-08) | 1 kit | 2016-12-29 | 0000-00-00 | No | No | Current |