NDC product
drospirenone and ethinyl estradiol
NDC 68462-720 · Glenmark Pharmaceuticals Inc., USA
Key facts
| Product NDC | 68462-720 |
|---|---|
| Proprietary name | drospirenone and ethinyl estradiol |
| Nonproprietary name | drospirenone and ethinyl estradiol |
| Dosage form | KIT |
| Labeler | Glenmark Pharmaceuticals Inc., USA |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA204296 |
| Marketing start | Aug 17, 2015 |
| Listing certified through | Dec 31, 2027 |
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: