GENERESS Fe
- Product NDC
- 52544-204
- 11-digit product format
- 525440204
- Labeler code
- 52544
- Product ID
- 52544-204_97bc8f12-a778-4679-8ad3-4e017dec8097
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- norethindrone and ethinyl estradiol and ferrous fumarate
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- NDA022573
- Marketing category
- NDA
- Marketing start
- 2011-12-23
- Marketing end
- 2019-10-31
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record