NDC product
Erlotinib
NDC 72485-219 · Armas Pharmaceuticals Inc.
Key facts
| Product NDC | 72485-219 |
|---|---|
| Proprietary name | Erlotinib |
| Nonproprietary name | Erlotinib hydrochloride |
| Substances | ERLOTINIB HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Armas Pharmaceuticals Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA211960 |
| Pharmacologic classes | Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA] |
| Marketing start | Nov 6, 2019 |
| 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: