Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate
- Product NDC
- 52544-058
- 11-digit product format
- 525440058
- Labeler code
- 52544
- Product ID
- 52544-058_f49b166c-00c1-46bf-b6f1-206df1ae29ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate
- Dosage form
- KIT
- Labeler
- Actavis Pharma, Inc.
- Application
- NDA203667
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-03-16
- Marketing end
- 2023-04-30
- 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 |
|---|
| 52544-058-72 | 52544005872 | 5 POUCH in 1 CARTON (52544-058-72) > 1 BLISTER PACK in 1 POUCH (52544-058-41) > 1 KIT in 1 BLISTER PACK | 5 pouch | 2017-03-16 | 0000-00-00 | No | No | Current |