Yaliira Pak
- Product NDC
- 69621-846
- 11-digit product format
- 696210846
- Labeler code
- 69621
- Product ID
- 69621-846_9db9f00e-236f-4198-882f-412c8016ad24
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- triamcinolone acetonide, dimethicone
- Dosage form
- KIT
- Labeler
- Shoreline Pharmaceuticals
- Application
- ANDA205373
- Marketing category
- ANDA
- Marketing start
- 2016-12-29
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record