NDC product
Aspirin and Dipyridamole
NDC 43598-339 · Dr. Reddy's Laboratories Inc
Key facts
| Product NDC | 43598-339 |
|---|---|
| Proprietary name | Aspirin and Dipyridamole |
| Nonproprietary name | Aspirin and Dipyridamole |
| Substances | ASPIRIN, DIPYRIDAMOLE |
| Dosage form | CAPSULE, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Dr. Reddy's Laboratories Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA209048 |
| Pharmacologic classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC] and 1 more |
| Marketing start | Oct 10, 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: