QUARTETTE
- Product NDC
- 51285-431
- 11-digit product format
- 512850431
- Labeler code
- 51285
- Product ID
- 51285-431_978c6012-75e6-438a-af3b-67bdf1ce1a88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levonorgestrel/Ethinyl Estradiol and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- Teva Women's Health, Inc.
- Application
- NDA204061
- Marketing category
- NDA
- Marketing start
- 2013-07-25
- 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 |
|---|
| 51285-431-65 | 51285043165 | 1 POUCH in 1 CARTON (51285-431-65) > 1 KIT in 1 POUCH | 1 pouch | 2013-07-25 | 0000-00-00 | No | No | Current |
| 51285-431-87 | 51285043187 | 2 POUCH in 1 CARTON (51285-431-87) > 1 KIT in 1 POUCH | 2 pouch | 2017-04-10 | 0000-00-00 | No | No | Current |