NDC product
TABLET, FILM COATED · Aurobindo Pharma Limited
NDC 65862-421 · Aurobindo Pharma Limited
Key facts
| Product NDC | 65862-421 |
|---|---|
| Nonproprietary name | Tenofovir Disoproxil Fumarate |
| Substances | TENOFOVIR DISOPROXIL FUMARATE |
| Dosage form | TABLET, FILM COATED |
| Labeler | Aurobindo Pharma Limited |
| Product type | DRUG FOR FURTHER PROCESSING |
| Marketing category | DRUG FOR FURTHER PROCESSING |
| Marketing start | Jan 26, 2018 |
| 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: