Quinixil
- Product NDC
- 72835-601
- 11-digit product format
- 728350601
- Labeler code
- 72835
- Product ID
- 72835-601_6508f6db-0e5e-46c7-a596-4bb5222a4d3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mometasone Furoate and Dimethicone
- Dosage form
- KIT
- Labeler
- V2 Pharma, LLC
- Application
- ANDA076216
- Marketing category
- ANDA
- Marketing start
- 2019-06-03
- Marketing end
- 0000-00-00
- Active strength
- 0
- 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 |
|---|
| 72835-601-02 | 72835060102 | 1 KIT in 1 CARTON (72835-601-02) * 114 g in 1 TUBE (69740-322-00) * 1 TUBE in 1 CARTON (0713-0634-37) > 45 g in 1 TUBE | 1 kit | 2019-06-03 | 0000-00-00 | No | No | Current |