Tretinopak
- Product NDC
- 59088-800
- 11-digit product format
- 590880800
- Labeler code
- 59088
- Product ID
- 59088-800_2b88164d-0cf1-4d8b-9c75-e44c28602850
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tretinoin, avobenzone, octinoxate, octisalate and titanium dioxide
- Dosage form
- KIT
- Labeler
- PureTek Corporation
- Application
- NDA020404
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-03-06
- 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