Treziopak
- Product NDC
- 59088-841
- 11-digit product format
- 590880841
- Labeler code
- 59088
- Product ID
- 59088-841_fad0ba68-f30b-4fde-ae7d-9dd9c89eb338
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- triamcinolone acetonide
- Dosage form
- KIT
- Labeler
- PureTek Corporation
- Application
- ANDA205373
- Marketing category
- ANDA
- Marketing start
- 2016-12-05
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record