Tilia Fe
- Product NDC
- 51862-284
- 11-digit product format
- 518620284
- Labeler code
- 51862
- Product ID
- 51862-284_ff2fca31-7d1e-4def-bef0-459ecd96745c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norethindrone Acetate and Ethinyl Estradiol
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- NDA020130
- Marketing category
- NDA
- Marketing start
- 2016-08-05
- Marketing end
- 2021-12-31
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 51862-284-03 | 51862028403 | 3 BLISTER PACK in 1 CARTON (51862-284-03) > 1 KIT in 1 BLISTER PACK (51862-284-01) | 3 blister pack | 2016-08-05 | 0000-00-00 | No | No | Current |