NDC product
leuprolide acetate
NDC 47335-936 · Sun Pharmaceutical Industries, Inc.
Key facts
| Product NDC | 47335-936 |
|---|---|
| Proprietary name | leuprolide acetate |
| Nonproprietary name | leuprolide acetate |
| Dosage form | KIT |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA078885 |
| Marketing start | Dec 15, 2014 |
| 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: