NDC product
Microgestin Fe 1/20
NDC 51862-866 · Mayne Pharma Inc.
Key facts
| Product NDC | 51862-866 |
|---|---|
| Proprietary name | Microgestin Fe 1/20 |
| Nonproprietary name | Norethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate |
| Dosage form | KIT |
| Labeler | Mayne Pharma Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA091454 |
| Marketing start | Oct 12, 2020 |
| 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: