norethindrone acetate and ethinyl estradiol and ferrous fumarate
- Product NDC
- 59762-1599
- 11-digit product format
- 597621599
- Labeler code
- 59762
- Product ID
- 59762-1599_66919340-bf0b-4c3c-9069-fc0416e8b86e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- norethindrone acetate and ethinyl estradiol, and ferrous fumarate
- Dosage form
- KIT
- Labeler
- Greenstone LLC
- Application
- NDA204426
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-02-28
- 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 |
|---|
| 59762-1599-5 | 59762159905 | 5 CARTON in 1 CARTON (59762-1599-5) > 1 BLISTER PACK in 1 CARTON (59762-1599-1) > 1 KIT in 1 BLISTER PACK | 5 carton | 2020-02-28 | 0000-00-00 | No | No | Current |