Mircette
- Product NDC
- 51285-120
- 11-digit product format
- 512850120
- Labeler code
- 51285
- Product ID
- 51285-120_85de2a58-5b5a-4bae-901b-2ca4f7d8533c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desogestrel/Ethinyl Estradiol and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- Teva Women's Health, Inc.
- Application
- ANDA075863
- Marketing category
- ANDA
- Marketing start
- 2014-09-15
- 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 |
|---|
| 51285-120-58 | 51285012058 | 6 POUCH in 1 CARTON (51285-120-58) > 1 BLISTER PACK in 1 POUCH (51285-120-79) > 1 KIT in 1 BLISTER PACK | 6 pouch | 2014-09-15 | 0000-00-00 | No | No | Current |