NDC product
Norethindrone and ethinyl estradiol and ferrous fumarate
NDC 79929-005 · Naari Pte Limited
Key facts
| Product NDC | 79929-005 |
|---|---|
| Proprietary name | Norethindrone and ethinyl estradiol and ferrous fumarate |
| Nonproprietary name | norethindrone and ethinyl estradiol and ferrous fumarate tablet |
| Dosage form | KIT |
| Labeler | Naari Pte Limited |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA207066 |
| Marketing start | Dec 31, 2022 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: